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103-11-7

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103-11-7 Usage

General Description

2-Ethylhexyl prop-2-enoate is an ester, specifically an ester of 2-ethylhexanol and propenoic acid (acrylic acid). It is commonly known as ethylhexyl acrylate and is widely used in the production of polymers and coatings.

Check Digit Verification of cas no

The CAS Registry Mumber 103-11-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,0 and 3 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 103-11:
(5*1)+(4*0)+(3*3)+(2*1)+(1*1)=17
17 % 10 = 7
So 103-11-7 is a valid CAS Registry Number.
InChI:InChI=1/C11H20O2/c1-4-7-8-10(5-2)9-13-11(12)6-3/h6,10H,3-5,7-9H2,1-2H3/t10-/m1/s1

103-11-7 Well-known Company Product Price

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  • Alfa Aesar

  • (L03854)  2-Ethylhexyl acrylate, 98%, stab.   

  • 103-11-7

  • 100ml

  • 198.0CNY

  • Detail
  • Alfa Aesar

  • (L03854)  2-Ethylhexyl acrylate, 98%, stab.   

  • 103-11-7

  • 500ml

  • 397.0CNY

  • Detail
  • Alfa Aesar

  • (L03854)  2-Ethylhexyl acrylate, 98%, stab.   

  • 103-11-7

  • 2500ml

  • 1133.0CNY

  • Detail
  • Sigma-Aldrich

  • (67262)  2-Ethylhexylacrylate  analytical standard

  • 103-11-7

  • 67262-5ML-F

  • 1,035.45CNY

  • Detail
  • Aldrich

  • (290815)  2-Ethylhexylacrylate  98%, contains ≥0.001-≤0.11% monomethyl ether hydroquinone as stabilizer

  • 103-11-7

  • 290815-25ML

  • 322.92CNY

  • Detail
  • Aldrich

  • (290815)  2-Ethylhexylacrylate  98%, contains ≥0.001-≤0.11% monomethyl ether hydroquinone as stabilizer

  • 103-11-7

  • 290815-1L

  • 436.41CNY

  • Detail
  • Aldrich

  • (290815)  2-Ethylhexylacrylate  98%, contains ≥0.001-≤0.11% monomethyl ether hydroquinone as stabilizer

  • 103-11-7

  • 290815-3L

  • 1,175.85CNY

  • Detail
  • Aldrich

  • (290815)  2-Ethylhexylacrylate  98%, contains ≥0.001-≤0.11% monomethyl ether hydroquinone as stabilizer

  • 103-11-7

  • 290815-18L

  • 4,998.24CNY

  • Detail

103-11-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Ethylhexyl acrylate

1.2 Other means of identification

Product number -
Other names Octyl Acrylate Monomer

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Adhesives and sealant chemicals,Intermediates,Paint additives and coating additives not described by other categories,Plasticizers,Solvents (which become part of product formulation or mixture)
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:103-11-7 SDS

103-11-7Synthetic route

2-Ethylhexyl alcohol
104-76-7

2-Ethylhexyl alcohol

acrylic acid methyl ester
292638-85-8

acrylic acid methyl ester

2-Ethylhexyl acrylate
103-11-7

2-Ethylhexyl acrylate

Conditions
ConditionsYield
With tetramethoxytitanium; 4-acetylamino-2,2,6,6-tetramethyl-1-piperidinoxy In 2-Methylpentane; cyclohexane at 90 - 110℃; for 6h;98%
2-Ethylhexyl alcohol
104-76-7

2-Ethylhexyl alcohol

acrylic acid
79-10-7

acrylic acid

2-Ethylhexyl acrylate
103-11-7

2-Ethylhexyl acrylate

Conditions
ConditionsYield
With hydroquinone at 115 - 180℃; for 4h; Reagent/catalyst; Inert atmosphere; Dean-Stark;83%
With hydroquinone In toluene at 93 - 94℃; under 375.038 Torr; for 6h; Pressure; Temperature; Flow reactor;80%
With alkanesulfonic acid; toluene at 120℃;
O-acetyl-lactic acid-(2-ethyl-hexyl ester)
500790-28-3

O-acetyl-lactic acid-(2-ethyl-hexyl ester)

2-Ethylhexyl acrylate
103-11-7

2-Ethylhexyl acrylate

Conditions
ConditionsYield
With pyrexglass at 500℃;
2-Ethylhexyl alcohol
104-76-7

2-Ethylhexyl alcohol

acrylic acid
79-10-7

acrylic acid

A

2-Ethylhexyl acrylate
103-11-7

2-Ethylhexyl acrylate

B

2-ethylhexyl β-2-ethylhexylhydroxypropionate
38940-91-9

2-ethylhexyl β-2-ethylhexylhydroxypropionate

Conditions
ConditionsYield
With KU-23 (10/60) sulphonic cation exchanger; hydroquinone at 90℃; Rate constant; Kinetics; Thermodynamic data; ΔH(excit.), ΔS(excit.), ΔG(excit.); var. sulphonic cation exchangers, var. temperatures;
2-Ethylhexyl alcohol
104-76-7

2-Ethylhexyl alcohol

acryloyl chloride
814-68-6

acryloyl chloride

2-Ethylhexyl acrylate
103-11-7

2-Ethylhexyl acrylate

Conditions
ConditionsYield
With triethylamine In chloroform at 10℃; for 12h;
In dichloromethane
2-Ethylhexyl alcohol
104-76-7

2-Ethylhexyl alcohol

acetylene
74-86-2

acetylene

carbon monoxide

carbon monoxide

2-Ethylhexyl acrylate
103-11-7

2-Ethylhexyl acrylate

Conditions
ConditionsYield
With 1-methyl-pyrrolidin-2-one; nickel dibromide at 190℃; under 20594.2 Torr;
With hydrogenchloride; tetracarbonyl nickel
With hydrogenchloride; tetracarbonyl nickel
diethyl ether dicarboxylic acid-(2.2')-bis-<2-ethyl-hexyl ester>

diethyl ether dicarboxylic acid-(2.2')-bis-<2-ethyl-hexyl ester>

2-Ethylhexyl acrylate
103-11-7

2-Ethylhexyl acrylate

Conditions
ConditionsYield
With sulfuric acid; hydroquinone at 189 - 205℃; under 34 - 36 Torr;
hydroxypropyl Acrylate

hydroxypropyl Acrylate

2-Ethylhexyl acrylate
103-11-7

2-Ethylhexyl acrylate

2-Ethylhexyl alcohol
104-76-7

2-Ethylhexyl alcohol

acrolein
107-02-8

acrolein

2-Ethylhexyl acrylate
103-11-7

2-Ethylhexyl acrylate

Conditions
ConditionsYield
Stage #1: acrolein With tert-butylhypochlorite In tetrachloromethane at 30℃; for 3.33333h;
Stage #2: 2-Ethylhexyl alcohol In tetrachloromethane at 50℃; for 0.5h;
trans-di-μ-acetato-bis ›o-(di-o-tolylphosphino)[benzyl]dipalladium

trans-di-μ-acetato-bis ›o-(di-o-tolylphosphino)[benzyl]dipalladium

2-Ethylhexyl acrylate
103-11-7

2-Ethylhexyl acrylate

para-bromoacetophenone
99-90-1

para-bromoacetophenone

2-ethylhexyl E-4-acetylcinnamate

2-ethylhexyl E-4-acetylcinnamate

Conditions
ConditionsYield
With sodium acetate In ISOPROPYLAMIDE100%
With sodium acetate In ISOPROPYLAMIDE100%
2-Ethylhexyl acrylate
103-11-7

2-Ethylhexyl acrylate

3-iodobenzoic acid methyl ester
58313-23-8

3-iodobenzoic acid methyl ester

ethyl (E)-3-(3-((2-ethylhexyl)oxy)-3-oxoprop-1-en-1-yl)benzoate

ethyl (E)-3-(3-((2-ethylhexyl)oxy)-3-oxoprop-1-en-1-yl)benzoate

Conditions
ConditionsYield
With potassium phosphate; sodium chloride In water; N,N-dimethyl-formamide at 45℃; for 16h; Micellar solution;100%
2-Ethylhexyl acrylate
103-11-7

2-Ethylhexyl acrylate

4-(N,N-diethylamino)benzenediazonium tetrafluoroborate
347-46-6

4-(N,N-diethylamino)benzenediazonium tetrafluoroborate

2'-ethylhexyl 4-N,N-diethylaminocinnamate

2'-ethylhexyl 4-N,N-diethylaminocinnamate

Conditions
ConditionsYield
[(1,3-dimesitylimidazol-2-ylidene)(naphthoquinone)Pd(0)]2 In methanol at 50℃; for 1h; Heck reaction;99%
(IMes)Pd(NQ) In ethanol at 50℃; for 1h; Conversion of starting material; Heck Reaction;99%
iodobenzene
591-50-4

iodobenzene

2-Ethylhexyl acrylate
103-11-7

2-Ethylhexyl acrylate

2-ethylhexyl cinnamate
16397-78-7

2-ethylhexyl cinnamate

Conditions
ConditionsYield
With (Bis(tri-tert-butylphosphine)palladium(0)); SPGS-550-M; NOK; triethylamine In water for 5h; Reagent/catalyst; Heck Reaction; Inert atmosphere; Sealed tube;99%
With triethylamine In N,N-dimethyl-formamide at 120℃; for 3h; Heck Reaction;90%
With potassium carbonate at 80℃; Heck Reaction; Micellar solution;82%
With potassium carbonate In N,N-dimethyl-formamide at 110℃; for 2h; Catalytic behavior; Heck Reaction; Inert atmosphere; Green chemistry;56%
With triethylamine at 80℃; for 18h; Heck reaction;68 %Spectr.
2-Ethylhexyl acrylate
103-11-7

2-Ethylhexyl acrylate

para-iodoanisole
696-62-8

para-iodoanisole

2-propenoic acid, 3-(4-methoxyphenyl)-, 2-ethylhexyl ester
5466-77-3

2-propenoic acid, 3-(4-methoxyphenyl)-, 2-ethylhexyl ester

Conditions
ConditionsYield
With water; potassium carbonate In 1-methyl-pyrrolidin-2-one at 135℃; for 24h; Catalytic behavior; Heck Reaction;99%
With tributyl-amine; palladium on activated charcoal; tetrabutylammomium bromide at 120℃; for 4h; Heck Reaction; Inert atmosphere;99 %Chromat.
N,N-dimethylindoline-1-carboxamide
61589-18-2

N,N-dimethylindoline-1-carboxamide

2-Ethylhexyl acrylate
103-11-7

2-Ethylhexyl acrylate

C22H32N2O3

C22H32N2O3

Conditions
ConditionsYield
With tetrafluoroboric acid; palladium diacetate; p-benzoquinone In ethyl acetate at 20℃; for 24h; Sealed tube;99%
2-Ethylhexyl acrylate
103-11-7

2-Ethylhexyl acrylate

C13H20N2O
128034-00-4

C13H20N2O

C24H38N2O3

C24H38N2O3

Conditions
ConditionsYield
With tetrafluoroboric acid; palladium diacetate; p-benzoquinone In ethyl acetate at 20℃; for 24h; Sealed tube;99%
2-Ethylhexyl acrylate
103-11-7

2-Ethylhexyl acrylate

2-methoxy-4-propenylphenol
97-54-1

2-methoxy-4-propenylphenol

(E)-2-ethylhexyl ferulate

(E)-2-ethylhexyl ferulate

Conditions
ConditionsYield
With Hoveyda-Grubbs catalyst first generation In 1,2-dichloro-ethane at 70℃; Cross Metathesis; Schlenk technique; Inert atmosphere; Glovebox;98%
2-Ethylhexyl acrylate
103-11-7

2-Ethylhexyl acrylate

3-carbethoxyphenyl halide

3-carbethoxyphenyl halide

ethyl (E)-3-(3-((2-ethylhexyl)oxy)-3-oxoprop-1-en-1-yl)benzoate

ethyl (E)-3-(3-((2-ethylhexyl)oxy)-3-oxoprop-1-en-1-yl)benzoate

Conditions
ConditionsYield
With potassium phosphate monohydrate; C64H118O20; sodium chloride In water at 20℃; Heck Reaction;98%
2-Ethylhexyl acrylate
103-11-7

2-Ethylhexyl acrylate

para-iodoanisole
696-62-8

para-iodoanisole

2-ethylhexyl methoxycinnamate
5466-77-3

2-ethylhexyl methoxycinnamate

Conditions
ConditionsYield
With tetrabutylammomium bromide; C32H26Cl2N8O4Pd2; potassium carbonate In methanol; water for 0.416667h; Reflux;97%
With C43H54NO5P; palladium diacetate; triethylamine In water at 40℃; for 12h; Heck Reaction;95%
With tributyl-amine; chloro-[2-(9-phenyl-1,10-phenanthrolin-2-yl)phenyl]palladium In 1-methyl-pyrrolidin-2-one at 140℃; for 15h; Heck Reaction; Inert atmosphere;94%
2-Ethylhexyl acrylate
103-11-7

2-Ethylhexyl acrylate

3-(3-methoxyphenyl)-1,1-dimethylurea
28170-54-9

3-(3-methoxyphenyl)-1,1-dimethylurea

C21H32N2O4

C21H32N2O4

Conditions
ConditionsYield
With tetrafluoroboric acid; palladium diacetate; p-benzoquinone In ethyl acetate at 20℃; for 24h; Sealed tube;97%
2-Ethylhexyl acrylate
103-11-7

2-Ethylhexyl acrylate

2-ethylhexyl glycidate
1609034-51-6

2-ethylhexyl glycidate

Conditions
ConditionsYield
With sodium hypochlorite; Aliquat 336; sodium hydrogencarbonate In aq. buffer at 40℃; for 1h; pH=8.2; Reagent/catalyst; Green chemistry;96.8%
2-Ethylhexyl acrylate
103-11-7

2-Ethylhexyl acrylate

4-methoxybenzenediazonium tetrafluoroborate
459-64-3

4-methoxybenzenediazonium tetrafluoroborate

2-ethylhexyl methoxycinnamate
5466-77-3

2-ethylhexyl methoxycinnamate

Conditions
ConditionsYield
[(1,3-dimesitylimidazol-2-ylidene)(benzoquinone)Pd(0)]2 In methanol at 50℃; for 1h; Heck reaction;96%
With calcium carbonate; Lindlar's catalyst In methanol93%
(IMes)Pd(NQ) In ethanol at 50℃; for 1h; Conversion of starting material; Heck Reaction;88%
palladium on activated carbon In dichloromethane; water; dimethyl sulfoxide80%
With xonotlite; palladium diacetate In methanol at 20℃; Reagent/catalyst;73%
2-Ethylhexyl acrylate
103-11-7

2-Ethylhexyl acrylate

4-nitrobenzenediazonium tetrafluoroborate
456-27-9

4-nitrobenzenediazonium tetrafluoroborate

2'-ethylhexyl 4-nitrocinnamate

2'-ethylhexyl 4-nitrocinnamate

Conditions
ConditionsYield
[(1,3-dimesitylimidazol-2-ylidene)(naphthoquinone)Pd(0)]2 In methanol at 50℃; for 1h; Heck reaction;96%
(IMes)Pd(NQ) In ethanol at 50℃; for 1h; Conversion of starting material; Heck Reaction;96%
1-nitro-4-(1-phenylbut-3-en-1-yloxy)benzene
1046862-39-8

1-nitro-4-(1-phenylbut-3-en-1-yloxy)benzene

2-Ethylhexyl acrylate
103-11-7

2-Ethylhexyl acrylate

(E)-2-ethylhexyl 5-(4-nitrophenoxy)-5-phenylpent-2-enoate
1046862-47-8

(E)-2-ethylhexyl 5-(4-nitrophenoxy)-5-phenylpent-2-enoate

Conditions
ConditionsYield
Grubbs-Hoveyda second generation catalyst In dichloromethane at 40℃; for 15h;96%
2-Ethylhexyl acrylate
103-11-7

2-Ethylhexyl acrylate

1-iodo-4-(3,7,11-trimethyldodecyloxy)benzene
1019205-88-9

1-iodo-4-(3,7,11-trimethyldodecyloxy)benzene

2-ethylhexyl (E)-3-(4-(3,7,11-trimethyldodecyloxy)phenyl)-acrylate
1019640-46-0

2-ethylhexyl (E)-3-(4-(3,7,11-trimethyldodecyloxy)phenyl)-acrylate

Conditions
ConditionsYield
With bis(tri-t-butylphosphine)palladium(0); toluene-4-sulfonic acid; triethylamine; sodium chloride In water at 22℃; for 3h; Heck coupling; Inert atmosphere;96%
With dichloro[1,1'-bis(di-t-butylphosphino)ferrocene]palladium(II); pyridinium p-toluenesulfonate; triethylamine In water at 50℃; under 760.051 Torr; for 8h; Heck reaction; Inert atmosphere; Micellar solution;94%
2-Ethylhexyl alcohol
104-76-7

2-Ethylhexyl alcohol

2-Ethylhexyl acrylate
103-11-7

2-Ethylhexyl acrylate

2-ethylhexyl β-2-ethylhexylhydroxypropionate
38940-91-9

2-ethylhexyl β-2-ethylhexylhydroxypropionate

Conditions
ConditionsYield
Stage #1: 2-Ethylhexyl alcohol With sodium at 60℃;
Stage #2: 2-Ethylhexyl acrylate at 60℃; for 12h;
96%
2-Ethylhexyl acrylate
103-11-7

2-Ethylhexyl acrylate

acetic acid-(3-propoxy-anilide)
55792-52-4

acetic acid-(3-propoxy-anilide)

C22H33NO4
1222482-58-7

C22H33NO4

Conditions
ConditionsYield
With tetrakis(acetonitrile)palladium(II) tetrafluoroborate; silver nitrate; p-benzoquinone In water at 20℃; for 20h; Fujiwara-Moritani reaction; regiospecific reaction;96%
2-Ethylhexyl acrylate
103-11-7

2-Ethylhexyl acrylate

2-ethylhexyl propionate
6293-37-4

2-ethylhexyl propionate

Conditions
ConditionsYield
With o-phenylenebis(diphenylphosphine); copper diacetate; poly(methylhydrosiloxane) In toluene; tert-butyl alcohol at 20℃; for 2h;95%
With 1,2,2,3,4,4-hexamethylphosphetane 1-oxide; phenylsilane; water In toluene at 80℃; for 24h; Schlenk technique; Inert atmosphere;61%
2-Ethylhexyl acrylate
103-11-7

2-Ethylhexyl acrylate

fenuron
101-42-8

fenuron

C20H30N2O3

C20H30N2O3

Conditions
ConditionsYield
With tetrafluoroboric acid; palladium diacetate; p-benzoquinone In ethyl acetate at 20℃; for 24h; Sealed tube;95%
decacarbonyldirhenium(0)
14285-68-8

decacarbonyldirhenium(0)

2-Ethylhexyl acrylate
103-11-7

2-Ethylhexyl acrylate

N-[1-(1-cyclohexen-1-yl)ethylidene]benzamine

N-[1-(1-cyclohexen-1-yl)ethylidene]benzamine

(C9H9CH3CO2CH2CH(C2H5)(CH2)3CH3)Re(CO)3

(C9H9CH3CO2CH2CH(C2H5)(CH2)3CH3)Re(CO)3

Conditions
ConditionsYield
In xylene byproducts: C9H10CH3CO2CH2CH(C2H5)(CH2)3CH3; xylene, 150°C, 72 h; as oil;94%
In toluene byproducts: C9H10CH3CO2CH2CH(C2H5)(CH2)3CH3; toluene, 150°C, 24 h;4%
2-phenyl-2,3-dihydro-1H-quinolin-4-one
16619-14-0

2-phenyl-2,3-dihydro-1H-quinolin-4-one

2-Ethylhexyl acrylate
103-11-7

2-Ethylhexyl acrylate

C26H31NO3

C26H31NO3

Conditions
ConditionsYield
With silver hexafluoroantimonate; [ruthenium(II)(η6-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]2; copper diacetate In 1,2-dichloro-ethane at 100℃; for 5h; chemoselective reaction;94%
2-Ethylhexyl acrylate
103-11-7

2-Ethylhexyl acrylate

para-bromobenzenethiol
106-53-6

para-bromobenzenethiol

3-(4-bromophenylsulfanyl)propionic acid 2-ethylhexyl ester
881664-08-0

3-(4-bromophenylsulfanyl)propionic acid 2-ethylhexyl ester

Conditions
ConditionsYield
With tetrabutyl ammonium fluoride In tetrahydrofuran at 20℃; for 15h;93%
2-Ethylhexyl acrylate
103-11-7

2-Ethylhexyl acrylate

1‐(but‐3‐en‐1‐yloxy)‐4‐nitrobenzene
40742-21-0

1‐(but‐3‐en‐1‐yloxy)‐4‐nitrobenzene

(E)-2-ethylhexyl 5-(4-nitrophenoxy)pent-2-enoate
1046862-42-3

(E)-2-ethylhexyl 5-(4-nitrophenoxy)pent-2-enoate

Conditions
ConditionsYield
Grubbs-Hoveyda second generation catalyst In dichloromethane at 40℃; for 15h;93%
2-Ethylhexyl acrylate
103-11-7

2-Ethylhexyl acrylate

3’H-spiro[indole-3,2’-[1,3]]benzothiazole-2(1H)-one
120105-59-1

3’H-spiro[indole-3,2’-[1,3]]benzothiazole-2(1H)-one

bis(2-ethylhexyl) 3,3'-(2'-oxo-3H-spiro[benzo[d]thiazole-2,3'-indoline]-1',3-diyl)dipropionate

bis(2-ethylhexyl) 3,3'-(2'-oxo-3H-spiro[benzo[d]thiazole-2,3'-indoline]-1',3-diyl)dipropionate

Conditions
ConditionsYield
With tetrabutylammomium bromide; potassium carbonate In neat (no solvent) at 20℃; for 3h; Michael Addition; Green chemistry; regioselective reaction;93%
poly(methacrylic acid)
79-41-4

poly(methacrylic acid)

2-Ethylhexyl acrylate
103-11-7

2-Ethylhexyl acrylate

poly(methacrylic acid-co-2-ethylhexyl acrylate)

poly(methacrylic acid-co-2-ethylhexyl acrylate)

Conditions
ConditionsYield
With dimethyl 2,2'-azobis(isobutyrate); 2,4-diphenyl-4-methyl-pent-1-ene In isopropyl alcohol at 80℃; for 20h;92.53%
tert-Octylamine
107-45-9

tert-Octylamine

2-Ethylhexyl acrylate
103-11-7

2-Ethylhexyl acrylate

para-iodoanisole
696-62-8

para-iodoanisole

2-ethylhexyl methoxycinnamate
5466-77-3

2-ethylhexyl methoxycinnamate

Conditions
ConditionsYield
With acetic acid; palladium on charcoal92%
palladium of charcoal

palladium of charcoal

2-Ethylhexyl acrylate
103-11-7

2-Ethylhexyl acrylate

para-iodoanisole
696-62-8

para-iodoanisole

2-ethylhexyl methoxycinnamate
5466-77-3

2-ethylhexyl methoxycinnamate

Conditions
ConditionsYield
With triethylamine In water; toluene92%
2-cyclohex-1-enyl-pyridine
14159-55-8

2-cyclohex-1-enyl-pyridine

2-Ethylhexyl acrylate
103-11-7

2-Ethylhexyl acrylate

2-ethylhexyl 3-[2-(2-pyridyl)-1-cyclohexenyl]propionate
1161621-73-3

2-ethylhexyl 3-[2-(2-pyridyl)-1-cyclohexenyl]propionate

Conditions
ConditionsYield
With bromotricarbonyl(tetrahydrofuran)rhenium(I) dimer In toluene at 135℃; for 24h; Inert atmosphere;91%

103-11-7Relevant articles and documents

Covalent Adaptable Networks Using β-Amino Esters as Thermally Reversible Building Blocks

Taplan, Christian,Guerre, Marc,Du Prez, Filip E.

, p. 9140 - 9150 (2021)

In this study, β-amino esters, prepared by the aza-Michael addition of an amine to an acrylate moiety, are investigated as building blocks for the formation of dynamic covalent networks. While such amino esters are usually considered as thermally nondynamic adducts, the kinetic model studies presented here show that dynamic covalent exchange occurs via both dynamic aza-Michael reaction and catalyst-free transesterification. This knowledge is transferred to create β-amino ester-based covalent adaptable networks (CANs) with coexisting dissociative and associative covalent dynamic exchange reactions. The ease, robustness, and versatility of this chemistry are demonstrated by using a variety of readily available multifunctional acrylates and amines. The presented CANs are reprocessed via either a dynamic aza-Michael reaction or a catalyst-free transesterification in the presence of hydroxyl moieties. This results in reprocessable, densely cross-linked materials with a glass transition temperature (Tg) ranging from -60 to 90 °C. Moreover, even for the low Tg materials, a high creep resistance was demonstrated at elevated temperatures up to 80 °C. When additional β-hydroxyl group-containing building blocks are applied during the network design, an enhanced neighboring group participation effect allows reprocessing of materials up to 10 times at 150 °C within 30 min while maintaining their material properties.

METHOD FOR PRODUCING UNSATURATED CARBOXYLIC ESTER

-

Paragraph 0064-0072, (2021/01/25)

An object of the present invention is to provide a method for producing an unsaturated carboxylic ester, wherein the risk of polymerization blockage is reduced and the required equipment cost and workload involved are kept low while maintaining a high conversion rate in an esterification reaction of unsaturated carboxylic acid. This object can be achieved by a method for producing an unsaturated carboxylic ester, which includes performing an esterification reaction using a reactor packed with a solid catalyst, wherein unsaturated carboxylic acid and alcohol are continuously fed to the reactor from an inlet thereof to form a fluid of the reaction solution in the reactor, and the vaporized organic solvent is continuously fed to the reactor from the inlet or a part near the inlet of the reactor.

PROCESS FOR PREPARING CARBOXYLIC ACID ESTERS IN THE PRESENCE OF A TITANIUM-CONTAINING CATALYST

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Page/Page column 16; 17; 18, (2016/04/09)

?The present invention relates to a process for preparing carboxylic acid esters, comprising esterification of a carboxylic acid with an alcohol in the presence of a titanium-containing catalyst selected from compounds of a general formula, Tin(OR)x(OR')xOy, wherein n is an integer from 1 to 4; у is an integer from 0 to 6; x can be the same or different and is an integer from 2 to 8; R is a linear or branched C1-C18alkyl, C3-C18cycloalkyl, R' is aryl optionally comprising an electron-donor substituent; or a mixture thereof, with the proviso that if n is 1, then x is 2 and у is 0; and if n>1, then the compounds comprise at least two alkoxy groups and two aryloxy groups. The present invention also relates to a process for preparing carboxylic acid esters, wherein a compound of general formula (I) or (II), wherein q represents an integer of 1 to 4; Y is independently R or R'; or a mixture thereof, with the proviso that the compounds comprise at least two alkoxy groups and two aryloxy groups, is used as a catalyst. The claimed process allows to reduce the amount of a used catalyst and the time of the process duration, while increasing the conversion rate of initial reagents and the yield of a target product.

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