Welcome to LookChem.com Sign In|Join Free

CAS

  • or

3699-54-5

Post Buying Request

3699-54-5 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

3699-54-5 Usage

Uses

1-(2-Hydroxyethyl)-2-imidazolidinone is one of the component in the formula of the environment-friendly water-based primer with the function of purifying air;Also, it is used in the preparation of a diatomite-supported formaldehyde scavenging agent.

General Description

1-(2-Hydroxyethyl)-2-imidazolidinone has been identified as monoethanolamine (MEA) degradation product in IMC Chemicals Facility in Trona, CA plant performing CO2 capture from flue gas. It was also identified from the MEA reclaimer from a CO2 capture facility product. It was also identified as the most stable thermal degradation product of MEA.

Flammability and Explosibility

Nonflammable

Check Digit Verification of cas no

The CAS Registry Mumber 3699-54-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,9 and 9 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3699-54:
(6*3)+(5*6)+(4*9)+(3*9)+(2*5)+(1*4)=125
125 % 10 = 5
So 3699-54-5 is a valid CAS Registry Number.
InChI:InChI=1/C5H10N2O2/c8-4-3-7-2-1-6-5(7)9/h8H,1-4H2,(H,6,9)

3699-54-5 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Aldrich

  • (378658)  1-(2-Hydroxyethyl)-2-imidazolidinonesolution  75% in H2O

  • 3699-54-5

  • 378658-250ML

  • 520.65CNY

  • Detail

3699-54-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-Hydroxyethyl)imidazolidin-2-one

1.2 Other means of identification

Product number -
Other names 1-(Hydroxyethyl)ethyleneurea

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Adhesives and sealant chemicals,Intermediates,Photosensitive chemicals
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:3699-54-5 SDS

3699-54-5Synthetic route

carbon dioxide
124-38-9

carbon dioxide

2-(2-Aminoethylamino)ethanol
111-41-1

2-(2-Aminoethylamino)ethanol

2-oxo-imidazolidine-1-ethanol
3699-54-5

2-oxo-imidazolidine-1-ethanol

Conditions
ConditionsYield
tetraphosphorus decasulfide; triphenyl antimony oxide In benzene at 150℃; under 36752.9 Torr; for 24h;95%
With alumina at 250℃; High pressure; Flow reactor; Supercritical conditions;70%
With ethylenediamine at 190℃; for 2h; Catalytic behavior; Reagent/catalyst; Temperature;
2-(2-Aminoethylamino)ethanol
111-41-1

2-(2-Aminoethylamino)ethanol

urea
57-13-6

urea

2-oxo-imidazolidine-1-ethanol
3699-54-5

2-oxo-imidazolidine-1-ethanol

Conditions
ConditionsYield
In 1,2-dimethoxyethane at 130℃; for 24h;89%
In ethylene glycol at 130℃; for 5h;70%
at 200℃;
carbon dioxide
124-38-9

carbon dioxide

ethanolamine
141-43-5

ethanolamine

2-oxo-imidazolidine-1-ethanol
3699-54-5

2-oxo-imidazolidine-1-ethanol

Conditions
ConditionsYield
With potassium phosphate In ethanol at 190℃; under 45004.5 Torr; for 6h; Reagent/catalyst; Temperature; Pressure; Autoclave;66.7%
With water at 165℃; under 30891.3 Torr;
carbon dioxide
124-38-9

carbon dioxide

ethanolamine
141-43-5

ethanolamine

A

dimethylenecyclourethane
497-25-6

dimethylenecyclourethane

B

2-oxo-imidazolidine-1-ethanol
3699-54-5

2-oxo-imidazolidine-1-ethanol

Conditions
ConditionsYield
at 180℃; under 75007.5 Torr; for 24h; Autoclave;A 3.5%
B 58.8%
ethanolamine
141-43-5

ethanolamine

urea
57-13-6

urea

2-oxo-imidazolidine-1-ethanol
3699-54-5

2-oxo-imidazolidine-1-ethanol

Conditions
ConditionsYield
With water at 170 - 180℃;
2-(2-Aminoethylamino)ethanol
111-41-1

2-(2-Aminoethylamino)ethanol

Diethyl carbonate
105-58-8

Diethyl carbonate

2-oxo-imidazolidine-1-ethanol
3699-54-5

2-oxo-imidazolidine-1-ethanol

Conditions
ConditionsYield
at 110 - 180℃;
2-(2-Aminoethylamino)ethanol
111-41-1

2-(2-Aminoethylamino)ethanol

2-oxo-imidazolidine-1-ethanol
3699-54-5

2-oxo-imidazolidine-1-ethanol

Conditions
ConditionsYield
With urea
With urea In water
With urea
concentrated ammonia water

concentrated ammonia water

conc. ammonia water

conc. ammonia water

2-(2-Aminoethylamino)ethanol
111-41-1

2-(2-Aminoethylamino)ethanol

1,8-diazabicyclo[5.4.0]undec-7-ene
6674-22-2

1,8-diazabicyclo[5.4.0]undec-7-ene

carbonic acid dimethyl ester
616-38-6

carbonic acid dimethyl ester

2-oxo-imidazolidine-1-ethanol
3699-54-5

2-oxo-imidazolidine-1-ethanol

Conditions
ConditionsYield
In methanol
2-(2-Aminoethylamino)ethanol
111-41-1

2-(2-Aminoethylamino)ethanol

carbonic acid dimethyl ester
616-38-6

carbonic acid dimethyl ester

2-oxo-imidazolidine-1-ethanol
3699-54-5

2-oxo-imidazolidine-1-ethanol

Conditions
ConditionsYield
With sodium methylate In methanol at 23 - 90℃; for 4h; Inert atmosphere;
With sodium methylate In methanol at 23 - 90℃; for 4h; Inert atmosphere;
dimethylenecyclourethane
497-25-6

dimethylenecyclourethane

imidazolidone
120-93-4

imidazolidone

ethylenediamine
107-15-3

ethylenediamine

A

2-oxo-imidazolidine-1-ethanol
3699-54-5

2-oxo-imidazolidine-1-ethanol

B

2-aminoethylimidazolidone
6281-42-1

2-aminoethylimidazolidone

C

U2TETA
166532-70-3

U2TETA

D

1,1'-(1,2-ethanediyl)di(2-imidazolidinone)
24368-15-8

1,1'-(1,2-ethanediyl)di(2-imidazolidinone)

E

U1TETA

U1TETA

F

1,5-diamino-3-azapentane
111-40-0

1,5-diamino-3-azapentane

G

triethylentetramine
112-24-3

triethylentetramine

Conditions
ConditionsYield
at 250℃; for 5.5h; Inert atmosphere;
dimethylenecyclourethane
497-25-6

dimethylenecyclourethane

imidazolidone
120-93-4

imidazolidone

ethylenediamine
107-15-3

ethylenediamine

A

2-oxo-imidazolidine-1-ethanol
3699-54-5

2-oxo-imidazolidine-1-ethanol

B

2-aminoethylimidazolidone
6281-42-1

2-aminoethylimidazolidone

C

2-(2-Aminoethylamino)ethanol
111-41-1

2-(2-Aminoethylamino)ethanol

D

1,5-diamino-3-azapentane
111-40-0

1,5-diamino-3-azapentane

E

triethylentetramine
112-24-3

triethylentetramine

Conditions
ConditionsYield
at 260℃; for 3h;
dimethylenecyclourethane
497-25-6

dimethylenecyclourethane

2-aminoethylimidazolidone
6281-42-1

2-aminoethylimidazolidone

A

2-oxo-imidazolidine-1-ethanol
3699-54-5

2-oxo-imidazolidine-1-ethanol

B

2-(2-Aminoethylamino)ethanol
111-41-1

2-(2-Aminoethylamino)ethanol

Conditions
ConditionsYield
at 280℃; for 5h; Microwave irradiation; Sealed tube; Inert atmosphere;
2-oxo-imidazolidine-1-ethanol
3699-54-5

2-oxo-imidazolidine-1-ethanol

Benzoylformic acid
611-73-4

Benzoylformic acid

PhGA-HEI

PhGA-HEI

Conditions
ConditionsYield
In water; acetone100%
2-oxo-imidazolidine-1-ethanol
3699-54-5

2-oxo-imidazolidine-1-ethanol

α-ketoglutaric acid
328-50-7

α-ketoglutaric acid

AKG-HEI

AKG-HEI

Conditions
ConditionsYield
In water; acetone100%
2-oxo-imidazolidine-1-ethanol
3699-54-5

2-oxo-imidazolidine-1-ethanol

1-(2-chloroethyl)imidazolidin-2-one
2387-20-4

1-(2-chloroethyl)imidazolidin-2-one

Conditions
ConditionsYield
With thionyl chloride In chloroform at 50℃;95%
With thionyl chloride In chloroform at 20℃; for 5h;68%
With thionyl chloride In dichloromethane at 20 - 40℃; for 3.08333h;66%
2-oxo-imidazolidine-1-ethanol
3699-54-5

2-oxo-imidazolidine-1-ethanol

methacrylic acid methyl ester
80-62-6

methacrylic acid methyl ester

A

N-(2-methacryloyloxyethyl)-N'-(methacryloyl) ethylene urea

N-(2-methacryloyloxyethyl)-N'-(methacryloyl) ethylene urea

B

2-(2-oxoimidazolidinyl)ethyl 2-methylprop-2-enoate

2-(2-oxoimidazolidinyl)ethyl 2-methylprop-2-enoate

Conditions
ConditionsYield
With TEMPOL; oxygen; di(n-butyl)tin oxide at 48 - 115℃; under 760.051 Torr; for 16.1667h; Product distribution / selectivity; Heating / reflux;A n/a
B 89.3%
With TEMPOL; oxygen; lithium hydroxide at 64 - 110℃; under 760.051 Torr; for 2.58333 - 21.5h; Product distribution / selectivity; Heating / reflux;A n/a
B 71.3%
Stage #1: 2-oxo-imidazolidine-1-ethanol; methacrylic acid methyl ester With TEMPOL; oxygen at 98℃; under 700 Torr; for 0.5h;
Stage #2: With lithium hydroxide; oxygen at 89 - 98℃; under 700 Torr; for 3h;
Stage #1: 2-oxo-imidazolidine-1-ethanol; methacrylic acid methyl ester With TEMPOL; oxygen at 95℃; under 700 Torr; for 0.25h;
Stage #2: With lithium hydroxide; oxygen at 90 - 96℃; under 700 Torr; for 2.5h;
Stage #1: 2-oxo-imidazolidine-1-ethanol; methacrylic acid methyl ester With TEMPOL; oxygen at 95℃; under 700 Torr; for 0.5h;
Stage #2: With lithium hydroxide; oxygen at 88 - 97℃; under 700 Torr; for 2.5h;
2-oxo-imidazolidine-1-ethanol
3699-54-5

2-oxo-imidazolidine-1-ethanol

2-fluoro-4-iodo-benzonitrile
137553-42-5

2-fluoro-4-iodo-benzonitrile

4-Iodo-2-(2-(2-oxoimidazolidinyl)-ethoxy)benzonitrile

4-Iodo-2-(2-(2-oxoimidazolidinyl)-ethoxy)benzonitrile

Conditions
ConditionsYield
With potassium hexamethylsilazane In tetrahydrofuran; toluene at 0 - 20℃;83%
2-oxo-imidazolidine-1-ethanol
3699-54-5

2-oxo-imidazolidine-1-ethanol

methacrylic acid methyl ester
80-62-6

methacrylic acid methyl ester

2-(2-oxoimidazolidinyl)ethyl 2-methylprop-2-enoate

2-(2-oxoimidazolidinyl)ethyl 2-methylprop-2-enoate

Conditions
ConditionsYield
With TEMPOL; oxygen; lithium hydroxide at 70 - 115℃; under 760.051 Torr; for 5.25h; Product distribution / selectivity; Heating / reflux;81%
With tempol; oxygen; potassium chloride; potassium carbonate at 98℃; under 550 - 700 Torr; for 3 - 4h; Product distribution / selectivity; Heating / reflux;
With tempol; oxygen; di(n-butyl)tin oxide at 98℃; under 700 Torr; for 1 - 4h; Product distribution / selectivity; Heating / reflux;
2-oxo-imidazolidine-1-ethanol
3699-54-5

2-oxo-imidazolidine-1-ethanol

meta-bromotoluene
591-17-3

meta-bromotoluene

1-(2-hydroxyethyl)-3-(m-tolyl)imidazolidin-2-one
1607801-94-4

1-(2-hydroxyethyl)-3-(m-tolyl)imidazolidin-2-one

Conditions
ConditionsYield
With di-tert-butyl(2,2-diphenyl-1-methyl-1-cyclopropyl)phosphine; bis(η3-allyl-μ-chloropalladium(II)); sodium t-butanolate In water at 50℃; for 18h; Buchwald-Hartwig Coupling; Inert atmosphere; chemoselective reaction;81%
rac-(trans-3,4)-4-(4-bromophenyl)pyrrolidine-3-carboxylic acid ethyl ester

rac-(trans-3,4)-4-(4-bromophenyl)pyrrolidine-3-carboxylic acid ethyl ester

2-oxo-imidazolidine-1-ethanol
3699-54-5

2-oxo-imidazolidine-1-ethanol

di(succinimido) carbonate
74124-79-1

di(succinimido) carbonate

(3R,4S)-4-(4-Bromo-phenyl)-pyrrolidine-1,3-dicarboxylic acid 3-ethyl ester 1-[2-(2-oxo-imidazolidin-1-yl)-ethyl] ester

(3R,4S)-4-(4-Bromo-phenyl)-pyrrolidine-1,3-dicarboxylic acid 3-ethyl ester 1-[2-(2-oxo-imidazolidin-1-yl)-ethyl] ester

Conditions
ConditionsYield
Stage #1: 2-oxo-imidazolidine-1-ethanol; di(succinimido) carbonate With triethylamine In acetonitrile at 20℃; for 4.5h;
Stage #2: rac-(trans-3,4)-4-(4-bromophenyl)pyrrolidine-3-carboxylic acid ethyl ester In acetonitrile at 20℃; for 3h;
80%
2-oxo-imidazolidine-1-ethanol
3699-54-5

2-oxo-imidazolidine-1-ethanol

5-fluoro-1-(2-fluorophenyl)-1H-indazol-3-ol
888952-52-1

5-fluoro-1-(2-fluorophenyl)-1H-indazol-3-ol

1-(2-(5-fluoro-1-(2-fluorophenyl)-1H-indazol-3-yloxy)ethyl)imidazolidin-2-one

1-(2-(5-fluoro-1-(2-fluorophenyl)-1H-indazol-3-yloxy)ethyl)imidazolidin-2-one

Conditions
ConditionsYield
With tributylphosphine; 1,1'-azodicarbonyl-dipiperidine In toluene at 80℃; Mitsunobu Displacement;80%
2-oxo-imidazolidine-1-ethanol
3699-54-5

2-oxo-imidazolidine-1-ethanol

4-Nitrophenyl chloroformate
7693-46-1

4-Nitrophenyl chloroformate

4-nitrophenyl (2-(2-oxoimidazolidin-1-yl)ethyl)carbonate
1386394-48-4

4-nitrophenyl (2-(2-oxoimidazolidin-1-yl)ethyl)carbonate

Conditions
ConditionsYield
With 4-methyl-morpholine In tetrahydrofuran for 1h;75%
2-oxo-imidazolidine-1-ethanol
3699-54-5

2-oxo-imidazolidine-1-ethanol

6-Benzyloxy-3-[3-methyl-4-[(1-pyrrolidinyl)methyl]-benzyl]-2-(4-hydroxyphenyl)benzo[b]thiophene
193966-06-2

6-Benzyloxy-3-[3-methyl-4-[(1-pyrrolidinyl)methyl]-benzyl]-2-(4-hydroxyphenyl)benzo[b]thiophene

6-Benzyloxy-3-[3-methyl-4-[(1-pyrrolidinyl)methyl]-benzyl]-2-[4-[2-(2-oxoimidazolidin-1-yl)ethoxy]phenyl]-benzo[b]thiophene
215388-35-5

6-Benzyloxy-3-[3-methyl-4-[(1-pyrrolidinyl)methyl]-benzyl]-2-[4-[2-(2-oxoimidazolidin-1-yl)ethoxy]phenyl]-benzo[b]thiophene

Conditions
ConditionsYield
With triethanolamine In tetrahydrofuran; SiO271%
2-oxo-imidazolidine-1-ethanol
3699-54-5

2-oxo-imidazolidine-1-ethanol

4-bromo-6-fluorobenzonitrile
105942-08-3

4-bromo-6-fluorobenzonitrile

4-bromo-2-(2-(2-oxoimidazolidin-1-yl)ethoxy)benzonitrile

4-bromo-2-(2-(2-oxoimidazolidin-1-yl)ethoxy)benzonitrile

Conditions
ConditionsYield
With potassium hexamethylsilazane In tetrahydrofuran at 20℃;71%
With potassium hexamethylsilazane In toluene at 20℃; for 18h;71%
2-oxo-imidazolidine-1-ethanol
3699-54-5

2-oxo-imidazolidine-1-ethanol

tert-butyldimethylsilyl chloride
18162-48-6

tert-butyldimethylsilyl chloride

1-(2-{[tert-butyl(dimethyl)silyl]oxy}ethyl)imidazolidin-2-one
864376-10-3

1-(2-{[tert-butyl(dimethyl)silyl]oxy}ethyl)imidazolidin-2-one

Conditions
ConditionsYield
With 1H-imidazole In N,N-dimethyl-formamide at 0 - 20℃;66%
With 1H-imidazole In N,N-dimethyl-formamide at 20℃; for 2h;
2-oxo-imidazolidine-1-ethanol
3699-54-5

2-oxo-imidazolidine-1-ethanol

triisopropylsilyl chloride
13154-24-0

triisopropylsilyl chloride

1-(2-triisopropylsilanyloxy-ethyl)-imidazolidin-2-one
1035140-40-9

1-(2-triisopropylsilanyloxy-ethyl)-imidazolidin-2-one

Conditions
ConditionsYield
With dmap; calcium hydride; triethylamine In dichloromethane; toluene at 20℃; for 16h; Inert atmosphere;60%
2-oxo-imidazolidine-1-ethanol
3699-54-5

2-oxo-imidazolidine-1-ethanol

1-chloro-3-(2-hydroxyethyl)imidazolidin-2-one
1373434-65-1

1-chloro-3-(2-hydroxyethyl)imidazolidin-2-one

Conditions
ConditionsYield
With tert-butylhypochlorite In methanol at 0℃; for 1.5h;60%
2-oxo-imidazolidine-1-ethanol
3699-54-5

2-oxo-imidazolidine-1-ethanol

p-chlorphenylisocyanate
104-12-1

p-chlorphenylisocyanate

C12H14ClN3O3

C12H14ClN3O3

Conditions
ConditionsYield
With triethylamine In acetonitrile at 20℃; for 24h;54%
2-oxo-imidazolidine-1-ethanol
3699-54-5

2-oxo-imidazolidine-1-ethanol

2-(2-oxoimidazolidin-1-yl)acetic acid
87219-22-5

2-(2-oxoimidazolidin-1-yl)acetic acid

Conditions
ConditionsYield
Stage #1: 2-oxo-imidazolidine-1-ethanol With 2,2,6,6-tetramethyl-piperidine-N-oxyl; sodium hydrogencarbonate; sodium bromide In water; acetone at 0℃; for 0.166667h;
Stage #2: With trichloroisocyanuric acid In water; acetone at 0 - 25℃; for 12h;
Stage #3: With hydrogenchloride In water pH=~ 2;
48%
2-oxo-imidazolidine-1-ethanol
3699-54-5

2-oxo-imidazolidine-1-ethanol

N-{(3E)-5-tert-butyl-1-methyl-2-[(2R)-tetrahydrofuran-2-ylmethyl]-1,2-dihydro-3H-pyrazol-3-ylidene}-2-fluoro-5-(trifluoromethyl)benzamide
1140917-51-6

N-{(3E)-5-tert-butyl-1-methyl-2-[(2R)-tetrahydrofuran-2-ylmethyl]-1,2-dihydro-3H-pyrazol-3-ylidene}-2-fluoro-5-(trifluoromethyl)benzamide

N-{(3E)-5-tert-butyl-1-methyl-2-[(2R)-tetrahydrofuran-2-ylmethyl]-1,2-dihydro-3H-pyrazol-3-ylidene}-2-[2-(2-oxoimidazolidin-1-yl)ethoxy]-5-(trifluoromethyl)benzamide
1217400-69-5

N-{(3E)-5-tert-butyl-1-methyl-2-[(2R)-tetrahydrofuran-2-ylmethyl]-1,2-dihydro-3H-pyrazol-3-ylidene}-2-[2-(2-oxoimidazolidin-1-yl)ethoxy]-5-(trifluoromethyl)benzamide

Conditions
ConditionsYield
Stage #1: 2-oxo-imidazolidine-1-ethanol With sodium hydride In tetrahydrofuran; mineral oil at -20℃; for 0.333333h;
Stage #2: N-{(3E)-5-tert-butyl-1-methyl-2-[(2R)-tetrahydrofuran-2-ylmethyl]-1,2-dihydro-3H-pyrazol-3-ylidene}-2-fluoro-5-(trifluoromethyl)benzamide In tetrahydrofuran; mineral oil at 20℃; for 20h;
48%
2-oxo-imidazolidine-1-ethanol
3699-54-5

2-oxo-imidazolidine-1-ethanol

methanesulfonyl chloride
124-63-0

methanesulfonyl chloride

2-(2-oxoimidazolidin-1-yl)ethyl methanesulfonate

2-(2-oxoimidazolidin-1-yl)ethyl methanesulfonate

Conditions
ConditionsYield
With triethylamine In dichloromethane Inert atmosphere;44%
With triethylamine In dichloromethane at 0 - 20℃; for 0.5h;
2-oxo-imidazolidine-1-ethanol
3699-54-5

2-oxo-imidazolidine-1-ethanol

trans-4-({6-[(6-bromo-1,3-benzothiazol-2-yl)amino]-4-[(2-methyl-1H-imidazol-1-yl)methyl]-2-pyridinyl}amino)cyclohexanol

trans-4-({6-[(6-bromo-1,3-benzothiazol-2-yl)amino]-4-[(2-methyl-1H-imidazol-1-yl)methyl]-2-pyridinyl}amino)cyclohexanol

1-[2-({6-[(trans-4-hydroxycyclohexyl)amino]-4-[(2-methyl-1H-imidazol-1-yl)methyl]-2-pyridinyl}amino)-1,3-benzothiazol-6-yl]-3-(2-hydroxyethyl)-2-imidazolidinone

1-[2-({6-[(trans-4-hydroxycyclohexyl)amino]-4-[(2-methyl-1H-imidazol-1-yl)methyl]-2-pyridinyl}amino)-1,3-benzothiazol-6-yl]-3-(2-hydroxyethyl)-2-imidazolidinone

Conditions
ConditionsYield
With caesium carbonate; N,N-dimethylethylenediamine; copper(l) iodide In N,N-dimethyl-formamide at 110℃; for 1h; Inert atmosphere;41%
2-oxo-imidazolidine-1-ethanol
3699-54-5

2-oxo-imidazolidine-1-ethanol

3,4-dichlorophenylisocyanate
102-36-3

3,4-dichlorophenylisocyanate

C12H13Cl2N3O3

C12H13Cl2N3O3

Conditions
ConditionsYield
With triethylamine In acetonitrile at 20℃; for 24h;39%
2-oxo-imidazolidine-1-ethanol
3699-54-5

2-oxo-imidazolidine-1-ethanol

p-toluenesulfonyl chloride
98-59-9

p-toluenesulfonyl chloride

2-(2-oxoimidazolidin-1-yl)ethyl 4-methylbenzenesulfonate

2-(2-oxoimidazolidin-1-yl)ethyl 4-methylbenzenesulfonate

Conditions
ConditionsYield
With pyridine at 0 - 20℃; for 16h; Inert atmosphere;33%
2-oxo-imidazolidine-1-ethanol
3699-54-5

2-oxo-imidazolidine-1-ethanol

methyl 4-(3-bromo-4-nitropyrazol-1-yl)benzoate

methyl 4-(3-bromo-4-nitropyrazol-1-yl)benzoate

methyl 4-[3-[3-(2-hydroxyethyl)-2-oxoimidazolidin-1-yl]-4-nitropyrazol-1-yl]benzoate

methyl 4-[3-[3-(2-hydroxyethyl)-2-oxoimidazolidin-1-yl]-4-nitropyrazol-1-yl]benzoate

Conditions
ConditionsYield
With potassium carbonate; N,N`-dimethylethylenediamine In 1,4-dioxane at 110℃; for 16h; Inert atmosphere;17%
2-oxo-imidazolidine-1-ethanol
3699-54-5

2-oxo-imidazolidine-1-ethanol

32-deoxo-rapamycin

32-deoxo-rapamycin

C16-(2-hydroxyethyl)-(2-oxoimidazolidin-1-yl)-C32-deoxorapamycin

C16-(2-hydroxyethyl)-(2-oxoimidazolidin-1-yl)-C32-deoxorapamycin

Conditions
ConditionsYield
With toluene-4-sulfonic acid In dichloromethane at 20℃;12%
2-oxo-imidazolidine-1-ethanol
3699-54-5

2-oxo-imidazolidine-1-ethanol

1,1'-(Azodicarbonyl)dipiperidin
10465-81-3

1,1'-(Azodicarbonyl)dipiperidin

4-(4-chloro-2-fluorophenylamino)-7-hydroxy-6-methoxyquinazoline
193001-59-1

4-(4-chloro-2-fluorophenylamino)-7-hydroxy-6-methoxyquinazoline

4-(4-chloro-2-fluoroanilino)-6-methoxy-7-(2-(2-oxoimidazolidin-1-yl)ethoxy)quinazoline
205193-70-0

4-(4-chloro-2-fluoroanilino)-6-methoxy-7-(2-(2-oxoimidazolidin-1-yl)ethoxy)quinazoline

Conditions
ConditionsYield
With tributylphosphine In dichloromethane6%
2-oxo-imidazolidine-1-ethanol
3699-54-5

2-oxo-imidazolidine-1-ethanol

6-((1-(cyclopropanecarbonyl)-4-hydroxypiperidin-4-yl)methyl)-3-(3-hydroxyphenyl)isothiazolo[4,5-d]pyrimidin-7(6H)-one

6-((1-(cyclopropanecarbonyl)-4-hydroxypiperidin-4-yl)methyl)-3-(3-hydroxyphenyl)isothiazolo[4,5-d]pyrimidin-7(6H)-one

1-[2-(3-{6-[(1-cyclopropanecarbonyl-4-hydroxypiperidin-4-yl)methyl]-7-oxo-6H,7H-[1,2]thiazolo[4,5-d]pyrimidin-3-yl}phenoxy)ethyl]imidazolidin-2-one

1-[2-(3-{6-[(1-cyclopropanecarbonyl-4-hydroxypiperidin-4-yl)methyl]-7-oxo-6H,7H-[1,2]thiazolo[4,5-d]pyrimidin-3-yl}phenoxy)ethyl]imidazolidin-2-one

Conditions
ConditionsYield
With triphenylphosphine; diethylazodicarboxylate In tetrahydrofuran at 0 - 23℃; for 16.25h;5%

3699-54-5Relevant articles and documents

PROCESS FOR MANUFACTURING A CYCLIC UREA ADDUCT OF AN ETHYLENEAMINE COMPOUND

-

Page/Page column 23-25, (2019/02/25)

The invention pertains to a process for manufacturing a cyclic urea adduct of an ethyleneamine compound, the ethyleneamine compound having a linear -NH-CH2-CH2-NH- group, the process comprising the steps of - in an absorption step contacting a liquid medium comprising an ethyleneamine compound having a linear -NH-CH2-CH2-NH- group with a CO2-containing gas stream at a pressure of 1 -20 bara, resulting in the formation of a liquid medium into which CO2 has been absorbed, - bringing the liquid medium to cyclic urea formation conditions, and in an urea formation step forming cyclic urea adduct of the ethyleneamine compound, urea formation conditions including a temperature of at least 120°C, wherein the total pressure at the end of the urea formation step is at most 20 bara, wherein the temperature in the absorption step is lower than the temperature in the urea formation step. It has been found that the process according to the invention makes it possible to obtain cyclic urea adducts in an efficient manner in the absence of metal-containing catalysts and to perform the process under relatively mild conditions, in particular relatively low pressure. More specifically, by separating the CO2 absorption step from the urea formation step, the CO2 absorption step can be carried out at relatively low temperatures and pressures. And because the CO2 is already present in the system at the beginning of the urea formation step, the pressure in the urea formation step does not need to be high.

PROCESS FOR PREPARING CYCLIC ALKYLENE UREAS

-

Page/Page column 17-19, (2019/02/25)

A process for producing a cyclic alkylene urea product of Formula I: in which a compound of Formula II and/or Formula III is contacted in a reaction zone with a compound of Formula IV and/or Formula V and in the presence of one or more carbonyl delivering compounds; in which; R1 is –[A?X?]qR3; R2 is on each occurrence independently selected from H and C1 to C6 alkyl groups which are optionally substituted by one or two groups selected from ?OH and ?NH2; R3 is on each occurrence independently selected from H and C1 to C6 alkyl groups which are optionally substituted by one or two groups selected from ?OH and ?NH2; A is on each occurrence independently selected from C1 to C3 alkylene units, optionally substituted by one or more C1 to C3 alkyl groups; X is on each occurrence independently selected from ?O?, ?NR2?, groups of Formula VI, and groups of Formula VII and p and q are each independently selected from a whole number in the range of from 0 to 8; wherein the compound of Formula II and/or the compound of Formula III are added to a reaction zone comprising compound of Formula IV and/or compound of Formula (V) continuously or semi-continuously over a period of time, or in two or more batches.

In order to CO2 As raw materials for preparing 1 - (2 - hydroxyethyl) - 2 - imidazolidinone method

-

Paragraph 0031-0037; 0038-0044; 0045-0051; 0053-0058, (2017/09/26)

The invention relates to the field of preparation of cyclic urea compounds, particularly to a method for preparing 1-(2-ethoxyl)-2-imidazolone by using CO2 as a raw material. 1-(2-ethoxyl)-2-imidazolone is obtained through a reaction of CO2 and ethanolamine. Compared with a conventional technology for preparing 1-(2-ethoxyl)-2-imidazolone, the method disclosed by the invention has the following advantages: (1) a synthetic method is scientific to design, an execution route is concise and reliable, and the method is suitable for industrial production; (2) required raw materials are low in toxicity, are cheap and are easy to obtain, so that the method conforms to the trend of green chemical development; (3) a catalyst is used in the reaction process, the catalytic activity is high, and the product yield is higher; (4) from the view of resources, the CO2 is a safe non-toxic rich carbon resource, and a reaction product, namely water, does not cause pressure to the environment.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 3699-54-5