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40150-98-9 Usage

Uses

4-(2-Methylpropyl)benzaldehyde is used in the synthesis of novel analgesis and antiimflammatory agents, inhibitors of COX-2 enzymes. Also used in the synthesis of inhibitors of breast cancer stem cells.

Check Digit Verification of cas no

The CAS Registry Mumber 40150-98-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,1,5 and 0 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 40150-98:
(7*4)+(6*0)+(5*1)+(4*5)+(3*0)+(2*9)+(1*8)=79
79 % 10 = 9
So 40150-98-9 is a valid CAS Registry Number.

40150-98-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Isobutylbenzaldehyde

1.2 Other means of identification

Product number -
Other names 4-sec-butylbenzaldehyde

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
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:40150-98-9 SDS

40150-98-9Synthetic route

(4-isobutyl-phenyl)-methanol
110319-85-2

(4-isobutyl-phenyl)-methanol

4-(2-methyl-1-propyl)benzaldehyde
40150-98-9

4-(2-methyl-1-propyl)benzaldehyde

Conditions
ConditionsYield
With pyridinium chlorochromate In dichloromethane for 3h;89%
N-Formylpiperidine
2591-86-8

N-Formylpiperidine

1-iodo-4-isobutylbenzene
85609-09-2

1-iodo-4-isobutylbenzene

4-(2-methyl-1-propyl)benzaldehyde
40150-98-9

4-(2-methyl-1-propyl)benzaldehyde

Conditions
ConditionsYield
With n-butyllithium84%
ibuprofen
15687-27-1

ibuprofen

A

4-(2-methyl-1-propyl)benzaldehyde
40150-98-9

4-(2-methyl-1-propyl)benzaldehyde

B

1-(4-isobutyl-phenyl)-ethanone
38861-78-8

1-(4-isobutyl-phenyl)-ethanone

C

2-(4-formylphenyl)propanoic acid
43153-07-7

2-(4-formylphenyl)propanoic acid

D

1-ethyl-4-(2-methylpropyl)benzene
100319-40-2

1-ethyl-4-(2-methylpropyl)benzene

E

1-(4-isobutylphenyl)ethanol
40150-92-3

1-(4-isobutylphenyl)ethanol

F

2-(4'-isobutyrylphenyl)propionic acid
65813-55-0

2-(4'-isobutyrylphenyl)propionic acid

Conditions
ConditionsYield
With 1,3,6,8-tetrahydro-2,4,5,7-pyrimido<5,4-g>pteridinetetrone; oxygen In acetonitrile for 3h; Product distribution; Mechanism; Ambient temperature; Irradiation; other reagents;A 2.2%
B 18%
C 1.7%
D n/a
E 37.1%
F 1.1%
4-isobutylaniline
30090-17-6

4-isobutylaniline

4-(2-methyl-1-propyl)benzaldehyde
40150-98-9

4-(2-methyl-1-propyl)benzaldehyde

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 84 percent / BuLi
View Scheme
1-(4-isobutyl-phenyl)-ethanone
38861-78-8

1-(4-isobutyl-phenyl)-ethanone

4-(2-methyl-1-propyl)benzaldehyde
40150-98-9

4-(2-methyl-1-propyl)benzaldehyde

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: 38 percent / aq. sodium hypochlorite / 12 h / Heating
2: borane / tetrahydrofuran / 3 h / Ambient temperature
3: 89 percent / pyridinium chlorochromate / CH2Cl2 / 3 h
View Scheme
4-isobutylbenzoic acid
38861-88-0

4-isobutylbenzoic acid

4-(2-methyl-1-propyl)benzaldehyde
40150-98-9

4-(2-methyl-1-propyl)benzaldehyde

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: borane / tetrahydrofuran / 3 h / Ambient temperature
2: 89 percent / pyridinium chlorochromate / CH2Cl2 / 3 h
View Scheme
Multi-step reaction with 2 steps
1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / N,N-dimethyl-formamide; acetonitrile
2: diisobutylaluminium hydride / toluene / -78 °C
View Scheme
Multi-step reaction with 2 steps
1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide; acetonitrile / 0 - 20 °C
2: diisobutylaluminium hydride / toluene / 0.33 h / -78 °C
View Scheme
1-phenyl-2-methylpropane
538-93-2

1-phenyl-2-methylpropane

carbon monoxide
201230-82-2

carbon monoxide

4-(2-methyl-1-propyl)benzaldehyde
40150-98-9

4-(2-methyl-1-propyl)benzaldehyde

Conditions
ConditionsYield
With methyl-cyclopentane; hydrogen fluoride; boron trifluoride at -25 - -15℃; under 15001.5 Torr; for 1.5h; Product distribution / selectivity;
With hydrogen fluoride; boron trifluoride at -25 - -15℃; under 15001.5 Torr; for 1.5h; Product distribution / selectivity;
1-phenyl-2-methylpropane
538-93-2

1-phenyl-2-methylpropane

4-(2-methyl-1-propyl)benzaldehyde
40150-98-9

4-(2-methyl-1-propyl)benzaldehyde

Conditions
ConditionsYield
With hydrogenchloride; aluminium trichloride In benzene
4-isobutyl-N-methoxy-N-methylbenzamide
1404380-23-9

4-isobutyl-N-methoxy-N-methylbenzamide

4-(2-methyl-1-propyl)benzaldehyde
40150-98-9

4-(2-methyl-1-propyl)benzaldehyde

Conditions
ConditionsYield
With diisobutylaluminium hydride In toluene at -78℃;
With diisobutylaluminium hydride In toluene at -78℃; for 0.333333h;
t-butyl bromide
507-19-7

t-butyl bromide

4-bromo-benzaldehyde
1122-91-4

4-bromo-benzaldehyde

A

4-(2-methyl-1-propyl)benzaldehyde
40150-98-9

4-(2-methyl-1-propyl)benzaldehyde

B

4-tert-Butylbenzaldehyde
939-97-9

4-tert-Butylbenzaldehyde

Conditions
ConditionsYield
With pyridine; bis(acetylacetonate)nickel(II); magnesium chloride; zinc; 1,3-diisopropyl-1H-imidazol-3-ium chloride In N,N-dimethyl acetamide at 25℃; for 12h; Reagent/catalyst; Inert atmosphere; Schlenk technique; Overall yield = 76 %; Overall yield = 37.1 mg;
[N-(p-tolylsulfonyl)imino]phenyliodinane
55962-05-5

[N-(p-tolylsulfonyl)imino]phenyliodinane

C22H28

C22H28

A

4-(2-methyl-1-propyl)benzaldehyde
40150-98-9

4-(2-methyl-1-propyl)benzaldehyde

B

C18H21NO2S

C18H21NO2S

Conditions
ConditionsYield
With water; palladium dichloride In chloroform at 20℃; for 6h;
(E)-4,4'-dibromostilbene
18869-30-2

(E)-4,4'-dibromostilbene

A

4-(2-methyl-1-propyl)benzaldehyde
40150-98-9

4-(2-methyl-1-propyl)benzaldehyde

B

C18H21NO2S

C18H21NO2S

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 1,3-bis[(diphenylphosphino)propane]dichloronickel(II) / diethyl ether / -20 - 20 °C / Reflux
2: palladium dichloride; water / chloroform / 6 h / 20 °C
View Scheme
carbon monoxide
201230-82-2

carbon monoxide

1-bromo-4-isobutylbenzene
2051-99-2

1-bromo-4-isobutylbenzene

4-(2-methyl-1-propyl)benzaldehyde
40150-98-9

4-(2-methyl-1-propyl)benzaldehyde

Conditions
ConditionsYield
With N,N,N,N,-tetramethylethylenediamine; hydrogen; palladium diacetate; catacxium A In toluene at 120℃; under 9000.9 Torr; Flow reactor; Green chemistry;53 %Chromat.
4-(2-methyl-1-propyl)benzaldehyde
40150-98-9

4-(2-methyl-1-propyl)benzaldehyde

o-hydroxyacetophenone
118-93-4

o-hydroxyacetophenone

C19H20O2

C19H20O2

Conditions
ConditionsYield
With potassium hydroxide In ethanol; water Claisen-Schmidt Condensation;100%
Stage #1: o-hydroxyacetophenone With sodium hydroxide In ethanol; water at 0 - 5℃;
Stage #2: 4-(2-methyl-1-propyl)benzaldehyde In ethanol; water
100%
With potassium hydroxide In ethanol; water
Stage #1: o-hydroxyacetophenone With sodium hydroxide In methanol for 0.5h;
Stage #2: 4-(2-methyl-1-propyl)benzaldehyde In methanol for 24h;
Stage #1: o-hydroxyacetophenone With sodium hydroxide In methanol; water at 20℃; for 0.5h; Claisen Condensation;
Stage #2: 4-(2-methyl-1-propyl)benzaldehyde In methanol; water at 20℃; for 4h; Claisen Condensation;
diethyl cyanophosphonate
2942-58-7

diethyl cyanophosphonate

4-(2-methyl-1-propyl)benzaldehyde
40150-98-9

4-(2-methyl-1-propyl)benzaldehyde

lithium cyanide
2408-36-8

lithium cyanide

cyano(4-isobutylphenyl)methyl diethylphosphate

cyano(4-isobutylphenyl)methyl diethylphosphate

Conditions
ConditionsYield
In tetrahydrofuran at 20℃; for 0.5h;98%
allyl 2-amino-2,2-diphenylacetate
946164-43-8

allyl 2-amino-2,2-diphenylacetate

4-(2-methyl-1-propyl)benzaldehyde
40150-98-9

4-(2-methyl-1-propyl)benzaldehyde

allyl (E)-2-((4-isobutylbenzylidene)amino)-2,2-diphenylacetate

allyl (E)-2-((4-isobutylbenzylidene)amino)-2,2-diphenylacetate

Conditions
ConditionsYield
In toluene at 130 - 150℃; Inert atmosphere; Dean-Stark;98%
4-(2-methyl-1-propyl)benzaldehyde
40150-98-9

4-(2-methyl-1-propyl)benzaldehyde

3-N-tert-butoxycarbonyl-3-(R)-aminopyrrolidine
122536-77-0

3-N-tert-butoxycarbonyl-3-(R)-aminopyrrolidine

C20H32N2O2
1000592-64-2

C20H32N2O2

Conditions
ConditionsYield
With sodium tris(acetoxy)borohydride In 1,2-dichloro-ethane at 23℃; for 12h;97%
4-(2-methyl-1-propyl)benzaldehyde
40150-98-9

4-(2-methyl-1-propyl)benzaldehyde

A

2-isopentylbenzaldehyde
1268267-77-1

2-isopentylbenzaldehyde

B

(4-isobutyl-phenyl)-methanol
110319-85-2

(4-isobutyl-phenyl)-methanol

Conditions
ConditionsYield
With aq NaOH In diethyl ether; waterA n/a
B 94%
4-(2-methyl-1-propyl)benzaldehyde
40150-98-9

4-(2-methyl-1-propyl)benzaldehyde

1,3-cylohexanedione
504-02-9

1,3-cylohexanedione

malononitrile
109-77-3

malononitrile

2-amino-5,6,7,8-tetrahydro-4-(4-isobutylphenyl)-5-oxo-4H-chromene-3-carbonitrile
1402044-73-8

2-amino-5,6,7,8-tetrahydro-4-(4-isobutylphenyl)-5-oxo-4H-chromene-3-carbonitrile

Conditions
ConditionsYield
With (2-hydroxyethyl)trimethylazanium urea chloride In neat (no solvent) at 20℃; for 0.416667h; Knoevenagel Condensation; Inert atmosphere; Green chemistry;93%
4-(2-methyl-1-propyl)benzaldehyde
40150-98-9

4-(2-methyl-1-propyl)benzaldehyde

N-Phenylglycine
103-01-5

N-Phenylglycine

1-(4-isobutylphenyl)-2-(phenylamino)ethan-1-ol

1-(4-isobutylphenyl)-2-(phenylamino)ethan-1-ol

Conditions
ConditionsYield
With (4,4'-di-tert-butyl-2,2'-dipyridyl)-bis-(2-phenylpyridine(-1H))-iridium(III) hexafluorophosphate In water at 20℃; for 3h; Schlenk technique; Inert atmosphere; Irradiation; Green chemistry;92%
4-(2-methyl-1-propyl)benzaldehyde
40150-98-9

4-(2-methyl-1-propyl)benzaldehyde

{[(difluoromethyl)selanyl]methyl}benzene

{[(difluoromethyl)selanyl]methyl}benzene

Se-(difluoromethyl) 4-isobutylbenzoselenoate

Se-(difluoromethyl) 4-isobutylbenzoselenoate

Conditions
ConditionsYield
With 2,2'-azobis(isobutyronitrile) In 1,2-dichloro-ethane at 50℃; for 24h; Inert atmosphere;92%
4-(2-methyl-1-propyl)benzaldehyde
40150-98-9

4-(2-methyl-1-propyl)benzaldehyde

S-(fluoromethyl) benzenesulfonothioate

S-(fluoromethyl) benzenesulfonothioate

S-(fluoromethyl)-4-isobutylbenzothioate

S-(fluoromethyl)-4-isobutylbenzothioate

Conditions
ConditionsYield
With 2,2'-azobis(isovaleronitrile) In 1,2-dichloro-ethane for 24h; Reflux;90%
4-(2-methyl-1-propyl)benzaldehyde
40150-98-9

4-(2-methyl-1-propyl)benzaldehyde

2-(diethylphosphono)propionic acid
30094-28-1

2-(diethylphosphono)propionic acid

(E)-3-(4-isobutylphenyl)-2-methylacrylic acid

(E)-3-(4-isobutylphenyl)-2-methylacrylic acid

Conditions
ConditionsYield
Stage #1: 2-(diethylphosphono)propionic acid With n-butyllithium In tetrahydrofuran; hexane at -60℃; for 1h; Horner-Wadsworth-Emmons Olefination; Inert atmosphere; Schlenk technique;
Stage #2: 4-(2-methyl-1-propyl)benzaldehyde In tetrahydrofuran; hexane at -60 - 20℃; Horner-Wadsworth-Emmons Olefination; Inert atmosphere; Schlenk technique; stereoselective reaction;
88%
terephthalonitrile
623-26-7

terephthalonitrile

4-(2-methyl-1-propyl)benzaldehyde
40150-98-9

4-(2-methyl-1-propyl)benzaldehyde

4-(hydroxy(4-isobutylphenyl)methyl)benzonitrile

4-(hydroxy(4-isobutylphenyl)methyl)benzonitrile

Conditions
ConditionsYield
With pentanal; tetrabutylammonium acetate In dimethyl sulfoxide at 50℃; for 6h; Electrochemical reaction;88%
C11H15FN2O2S
1000592-50-6

C11H15FN2O2S

4-(2-methyl-1-propyl)benzaldehyde
40150-98-9

4-(2-methyl-1-propyl)benzaldehyde

C22H29FN2O2S
1000592-51-7

C22H29FN2O2S

Conditions
ConditionsYield
With sodium tris(acetoxy)borohydride87%
malonic acid
141-82-2

malonic acid

4-(2-methyl-1-propyl)benzaldehyde
40150-98-9

4-(2-methyl-1-propyl)benzaldehyde

4-isobutylcinnamic acid
66734-95-0

4-isobutylcinnamic acid

Conditions
ConditionsYield
With morpholine for 2h; Heating;86%
4-(2-methyl-1-propyl)benzaldehyde
40150-98-9

4-(2-methyl-1-propyl)benzaldehyde

ethyl acetoacetate
141-97-9

ethyl acetoacetate

urea
57-13-6

urea

ethyl 1,2,3,4-tetrahydro-4-(4-isobutylphenyl)-6-methyl-2-oxopyrimidine-5-carboxylate
329778-25-8

ethyl 1,2,3,4-tetrahydro-4-(4-isobutylphenyl)-6-methyl-2-oxopyrimidine-5-carboxylate

Conditions
ConditionsYield
With 2,2,2-trifluoroethanol at 80℃; Biginelli pyrimidine synthesis;85%
4-(2-methyl-1-propyl)benzaldehyde
40150-98-9

4-(2-methyl-1-propyl)benzaldehyde

7-((3-(diethylamino)propyl)amino)-6-fluoro-2-methylquinazolin-4(3H)-one

7-((3-(diethylamino)propyl)amino)-6-fluoro-2-methylquinazolin-4(3H)-one

(E)-7-((3-(diethylamino)propyl)amino)-6-fluoro-2-(4-isobutylstyryl)quinazolin-4(3H)-one

(E)-7-((3-(diethylamino)propyl)amino)-6-fluoro-2-(4-isobutylstyryl)quinazolin-4(3H)-one

Conditions
ConditionsYield
With chloro-trimethyl-silane In N,N-dimethyl-formamide at 100℃; Knoevenagel Condensation; Sealed tube;85%
4-(2-methyl-1-propyl)benzaldehyde
40150-98-9

4-(2-methyl-1-propyl)benzaldehyde

4-isobutylbenzaldehyde oxime
179675-04-8

4-isobutylbenzaldehyde oxime

Conditions
ConditionsYield
With pyridine; hydroxylamine hydrochloride In ethanol at 20℃; for 18h;84%
4-(2-methyl-1-propyl)benzaldehyde
40150-98-9

4-(2-methyl-1-propyl)benzaldehyde

Methyltriphenylphosphonium bromide
1779-49-3

Methyltriphenylphosphonium bromide

p-isobutylstyrene
63444-56-4

p-isobutylstyrene

Conditions
ConditionsYield
With potassium carbonate In 1,4-dioxane for 16h; Reflux;84%
Stage #1: Methyltriphenylphosphonium bromide With n-butyllithium In tetrahydrofuran; hexane at 0℃; for 2h; Schlenk technique;
Stage #2: 4-(2-methyl-1-propyl)benzaldehyde In tetrahydrofuran at 0 - 20℃;
81%
Stage #1: Methyltriphenylphosphonium bromide With n-butyllithium In tetrahydrofuran; hexane; cyclohexane at 0℃; for 4h; Inert atmosphere;
Stage #2: 4-(2-methyl-1-propyl)benzaldehyde In tetrahydrofuran; hexane; cyclohexane at 20℃; for 10h; Wittig Olefination; Inert atmosphere;
75%
With potassium tert-butylate In tetrahydrofuran Inert atmosphere;
4-(2-methyl-1-propyl)benzaldehyde
40150-98-9

4-(2-methyl-1-propyl)benzaldehyde

S-(trifluoromethyl) benzenesulfonothioate
15398-96-6

S-(trifluoromethyl) benzenesulfonothioate

S-(trifluoromethyl)-4-isobutylbenzothioate

S-(trifluoromethyl)-4-isobutylbenzothioate

Conditions
ConditionsYield
With 2,2'-azobis(isobutyronitrile) In 1,2-dichloro-ethane at 80℃; for 16h; Irradiation;83%
4-(2-methyl-1-propyl)benzaldehyde
40150-98-9

4-(2-methyl-1-propyl)benzaldehyde

trimethyl(phenyl)stannane
934-56-5

trimethyl(phenyl)stannane

(4-isobutylphenyl)(phenyl)methanol

(4-isobutylphenyl)(phenyl)methanol

Conditions
ConditionsYield
With bis(acetonitrile)(1,5-cyclooctadiene)rhodium(I) tetrafluoroborate In tetrahydrofuran at 60℃; for 20h;78%
4-(2-methyl-1-propyl)benzaldehyde
40150-98-9

4-(2-methyl-1-propyl)benzaldehyde

(methoxymethyl)triphenylphosphonium chloride
4009-98-7

(methoxymethyl)triphenylphosphonium chloride

2-­(6-­methoxynaphthalen-­2-­yl)acetaldehyde

2-­(6-­methoxynaphthalen-­2-­yl)acetaldehyde

Conditions
ConditionsYield
Stage #1: (methoxymethyl)triphenylphosphonium chloride With potassium tert-butylate In tetrahydrofuran at 0℃; for 0.75h; Inert atmosphere;
Stage #2: 4-(2-methyl-1-propyl)benzaldehyde In tetrahydrofuran at 20℃; for 1h; Inert atmosphere;
77%
4-(2-methyl-1-propyl)benzaldehyde
40150-98-9

4-(2-methyl-1-propyl)benzaldehyde

4-phenyl-but-3-yn-1-ol
10229-11-5

4-phenyl-but-3-yn-1-ol

benzene
71-43-2

benzene

2-(1-(4-isobutylphenyl)-3-phenyl-1H-inden-2-yl)ethanol

2-(1-(4-isobutylphenyl)-3-phenyl-1H-inden-2-yl)ethanol

Conditions
ConditionsYield
With boron trifluoride diethyl etherate at 0 - 25℃; for 1h; Inert atmosphere;76%
4-(2-methyl-1-propyl)benzaldehyde
40150-98-9

4-(2-methyl-1-propyl)benzaldehyde

phenylmethanethiol
100-53-8

phenylmethanethiol

p-Chlorothiophenol
106-54-7

p-Chlorothiophenol

A

benzyl(((4-chlorophenyl)thio)(4-isobutylphenyl)methyl)sulfane

benzyl(((4-chlorophenyl)thio)(4-isobutylphenyl)methyl)sulfane

B

C25H28S2

C25H28S2

C

C23H22Cl2S2

C23H22Cl2S2

Conditions
ConditionsYield
With camphor-10-sulfonic acid In ethyl acetate at 20℃; for 6h; Schlenk technique; Overall yield = 94 percent; Overall yield = 0.39 g;A 76%
B n/a
C n/a
4-(2-methyl-1-propyl)benzaldehyde
40150-98-9

4-(2-methyl-1-propyl)benzaldehyde

isobutyltriphenylphosphonium bromide
22884-29-3

isobutyltriphenylphosphonium bromide

A

Z-1-iso-butyl-4-(3-methylbut-1-en-1-yl)benzene

Z-1-iso-butyl-4-(3-methylbut-1-en-1-yl)benzene

B

E-1-iso-butyl-4-(3-methylbut-1-en-1-yl)benzene

E-1-iso-butyl-4-(3-methylbut-1-en-1-yl)benzene

Conditions
ConditionsYield
Stage #1: isobutyltriphenylphosphonium bromide With n-butyllithium In tetrahydrofuran; hexane at 0℃; for 2h; Schlenk technique;
Stage #2: 4-(2-methyl-1-propyl)benzaldehyde In tetrahydrofuran at 0 - 20℃; Overall yield = 75 %; Overall yield = 1.52 g;
A n/a
B 75%
4-(2-methyl-1-propyl)benzaldehyde
40150-98-9

4-(2-methyl-1-propyl)benzaldehyde

7-fluoro-6-((2-(piperidin-1-yl)ethyl)amino)-2,3-dihydropyrrolo-[2,1-b]quinazolin-9(1H)-one

7-fluoro-6-((2-(piperidin-1-yl)ethyl)amino)-2,3-dihydropyrrolo-[2,1-b]quinazolin-9(1H)-one

(E)-3-(4-isobutylbenzylidene)-7-fluoro-6-((2-(piperidin-1-yl)-ethyl)amino)-2,3-dihydropyrrolo[2,1-b]quinazolin-9(1H)-one

(E)-3-(4-isobutylbenzylidene)-7-fluoro-6-((2-(piperidin-1-yl)-ethyl)amino)-2,3-dihydropyrrolo[2,1-b]quinazolin-9(1H)-one

Conditions
ConditionsYield
With chloro-trimethyl-silane In N,N-dimethyl-formamide at 100℃; Sealed tube;71%
4-(2-methyl-1-propyl)benzaldehyde
40150-98-9

4-(2-methyl-1-propyl)benzaldehyde

(4-chlorphenyl)magnesium bromide
873-77-8

(4-chlorphenyl)magnesium bromide

(4-chlorophenyl)-(4-isobutylphenyl)methanol
660840-75-5

(4-chlorophenyl)-(4-isobutylphenyl)methanol

Conditions
ConditionsYield
Stage #1: 4-(2-methyl-1-propyl)benzaldehyde; (4-chlorphenyl)magnesium bromide In diethyl ether at 0 - 20℃; for 2.5h;
Stage #2: With hydrogenchloride In diethyl ether; water
69%
4-(2-methyl-1-propyl)benzaldehyde
40150-98-9

4-(2-methyl-1-propyl)benzaldehyde

methoxybenzene
100-66-3

methoxybenzene

5-isobutyl-4'-methoxy-[1,1'-biphenyl]-2-carbaldehyde

5-isobutyl-4'-methoxy-[1,1'-biphenyl]-2-carbaldehyde

Conditions
ConditionsYield
With dipotassium peroxodisulfate; palladium diacetate; 2-Aminoisobutyric acid; trifluoroacetic acid at 60℃; for 24h; Sealed tube; regioselective reaction;63%
8-chloro-2,3-dihydro-1H-cyclopenta[1,2-b]quinoline
40528-00-5

8-chloro-2,3-dihydro-1H-cyclopenta[1,2-b]quinoline

4-(2-methyl-1-propyl)benzaldehyde
40150-98-9

4-(2-methyl-1-propyl)benzaldehyde

(E)-9-chloro-3-(4-isobutylbenzylidene)-2,3-dihydro-1H-cyclopenta[b]quinoline

(E)-9-chloro-3-(4-isobutylbenzylidene)-2,3-dihydro-1H-cyclopenta[b]quinoline

Conditions
ConditionsYield
With chloro-trimethyl-silane In N,N-dimethyl-formamide at 100℃; Knoevenagel Condensation; Sealed tube;62%
danishefsky's diene
54125-02-9

danishefsky's diene

4-(2-methyl-1-propyl)benzaldehyde
40150-98-9

4-(2-methyl-1-propyl)benzaldehyde

2-(4-isobutyl-phenyl)-2,3-dihydro-pyran-4-one

2-(4-isobutyl-phenyl)-2,3-dihydro-pyran-4-one

Conditions
ConditionsYield
With Ce(III)-(R)-BNP In dichloromethane at 20℃; for 15h; asymmetric hetero-Diels-Alder reaction;61%

40150-98-9Relevant articles and documents

Continuous-flow Synthesis of Aryl Aldehydes by Pd-catalyzed Formylation of Aryl Bromides Using Carbon Monoxide and Hydrogen

Hone, Christopher A.,Lopatka, Pavol,Munday, Rachel,O'Kearney-McMullan, Anne,Kappe, C. Oliver

, p. 326 - 337 (2018/11/23)

A continuous-flow protocol utilizing syngas (CO and H2) was developed for the palladium-catalyzed reductive carbonylation of (hetero)aryl bromides to their corresponding (hetero)aryl aldehydes. The optimization of temperature, pressure, catalyst and ligand loading, and residence time resulted in process-intensified flow conditions for the transformation. In addition, a key benefit of investigating the reaction in flow is the ability to precisely control the CO-to-H2 stoichiometric ratio, which was identified as having a critical influence on yield. The protocol proceeds with low catalyst and ligand loadings: palladium acetate (1 mol % or below) and cataCXium A (3 mol % or below). A variety of (hetero)aryl bromides at a 3 mmol scale were converted to their corresponding (hetero)aryl aldehydes at 12 bar pressure (CO/H2=1:3) and 120 °C reaction temperature within 45 min residence time to afford products mostly in good-to-excellent yields (17 examples). In particular, a successful scale-up was achieved over 415 min operation time for the reductive carbonylation of 2-bromo-6-methoxynaphthalene to synthesize 3.8 g of 6-methoxy-2-naphthaldehyde in 85 % isolated yield. Studies were conducted to understand catalyst decomposition within the reactor by using inductively coupled plasma–mass spectrometry (ICP–MS) analysis. The palladium could easily be recovered using an aqueous nitric acid wash post reaction. Mechanistic aspects and the scope of the transformation are discussed.

Metal-catalyzed formal amidation of alkenes under CO-free condition

Zhang, Yuanyuan,Ye, Wenjing,Leng, Xue,He, Ying,Zhang, Hui,Xiao, Xiao

, p. 4203 - 4206 (2016/08/24)

An effective procedure for synthesis of amides from alkenes and [Formula presented] via Pd and Fe catalysts under mild conditions is described. A series of benzamides containing various functional groups can be obtained in reasonable yield and the possible reaction pathway is proposed in this Letter.

AMIDE COMPOUND AND MEDICINAL USE THEREOF

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Page/Page column 108, (2013/02/27)

A compound of formula [I-W]: wherein each symbol is as defined in the description, or a pharmaceutically acceptable salt thereof.

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