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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 729441Generated: October 30, 2026

2-(Bromomethyl)acrylic acid ethyl ester → Ethyl 2-(methoxymethyl)prop-2-enoate

https://huagongshe.com/reaction/729441

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Bromomethyl)acrylic acid ethyl esterHCID 310620—
ReactantSodium MethoxideHCID 10942334—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductEthyl 2-(methoxymethyl)prop-2-enoateHCID 2077013428.7%

Reaction Steps

A solution of ethyl α-(bromomethyl)acrylate (0.99 g, 5.1 mmol [Villieras J., Rambaud M., Synthesis, 1982:924-926]) in methanol (10 mL) is added to an ice-cold solution of sodium methoxide (0.33 g, 6.1 mmol) in methanol (50 mL). The suspension is refluxed for 21 hours, cooled, diluted with water and extracted with dichloromethane. The organic extracts are dried over Na2SO4, filtered and concentrated under vacuum. The resulting residue is purified by flash column chromatography (1:5 ethyl acetate/hexanes) to afford the title compound (0.211 g). 1H NMR (200 MHz, CDCl3): δ 6.33-6.26 (m, 1H), 5.88-5.80 (m, 1H), 4.23 (q, 2H), 4.19-4.10 (m, 2H), 3.41 (s, 311), 1.31 (t, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582627B2
Source datasetuspto-grants-2009_09
ORD IDord-2878eb458ef34ba6a77771ed4785578b
Source noteuspto-grants-2009_09