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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1901437Generated: October 30, 2026

3-Butenoic acid → 3-Butenoic acid 2-(4-phenoxyphenoxy)-ethyl ester

https://huagongshe.com/reaction/1901437

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Butenoic acidHCID 32743—
Reactant2-(4-Phenoxyphenoxy)ethanolHCID 4676725—
Catalyst4-PyrrolidinopyridineHCID 75567—
SolventDichloromethaneHCID 6344—
Product3-Butenoic acid 2-(4-phenoxyphenoxy)-ethyl esterHCID 5416626889.5%

Reaction Steps

0.05 g of 4-pyrrolidinopyridine and 17.25 g of 2-(4-phenoxyphenoxy)-ethanol are added at room temperature, with stirring, to a solution of 6.45 g of 3-butenoic acid in 100 ml of dichloromethane. At a temperature of 0° C., 17.0 g (82.5 mmol) of N,N-dicyclohexylcarbodiimide are then added in portions, and the reaction mixture is stirred at room temperature for 3 hours. The reaction mixture is filtered. The precipitate which has been separated off is discarded, and the filtrate is washed with water and dried over sodium sulfate. After concentration by evaporation, the oily residue is purified by column chromatography on silica gel with hexane/ethyl acetate (9:1), yielding 20.0 g of 3-butenoic acid 2-(4-phenoxyphenoxy)-ethyl ester of the formula ##STR12## in the form of a colourless oil having a refractive index of nD23 : 1.5538.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05578595
Source datasetuspto-grants-1996_11
ORD IDord-1376f5abcff54a9db7fef69f06fb77dd
Source noteuspto-grants-1996_11