2-Hydroxyethyl acrylate → 2-Hydroxyethyl acrylate dodecyl acrylate

HRID 65657

Reaction equation

HRID 65657 reaction equation
[C:1]([O:5][CH2:6][CH2:7][OH:8])(=[O:4])[CH:2]=[CH2:3].[C:9]([O:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH3:25])(=[O:12])[CH:10]=[CH2:11]>C(C(C)=O)C.C(OOC(=O)C1C=CC=CC=1)(=O)C1C=CC=CC=1>[C:1]([O:5][CH2:6][CH2:7][OH:8])(=[O:4])[CH:2]=[CH2:3].[C:9]([O:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH3:25])(=[O:12])[CH:10]=[CH2:11]

Participants

5

Conditions

Temperature
80 °C

Procedure

11.6 gm (0.1 mole) of 2-hydroxyethyl acrylate and 144 gm (0.6 mole) of dodecyl acrylate were dissolved in 360 gm of methyl ethyl ketone. To the solution obtained were added 3.1 gm of dibenzoyl peroxide as a catalyst. The reaction mixture was maintained for 5 hours under stirring at a temperature of 80° C. After the reaction was completed, the solvent was distilled off and the reaction product was washed several times with methanol. 148 gm, (95% of theory) of 2-hydroxyethyl acrylate/dodecyl acrylate copolymer (1:6 molar ratio) were obtained.

Workup

  1. customTo the solution obtained
  2. temperatureThe reaction mixture was maintained for 5 hours
  3. distillationthe solvent was distilled off
  4. washthe reaction product was washed several times with methanol

Sources & evidence

ORD record
ord-2bbc4b23c5c64a3ab005af79ef0409da
Source dataset
uspto-grants-1978_12
Patent number
US04128635

Linked notes

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