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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 648559Generated: October 26, 2026

Hydrochloric Acid → Methyl 3-hydroxy-2-(alpha,alpha,alpha-trifluoro-m-tolyl)acrylate

https://huagongshe.com/reaction/648559

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethyl formateHCID 7865—
ReactantMethyl (3-(trifluoromethyl)phenyl)acetateHCID 2734603—
ReactantSodiumHCID 5360545—
SolventDiethyl EtherHCID 3283—
ProductMethyl 3-hydroxy-2-(alpha,alpha,alpha-trifluoro-m-tolyl)acrylateHCID 67828062—

Reaction Steps

(aa) 26.2 g of methyl 3-trifluoromethylphenylacetate were dissolved in 100 ml of diethyl ether and, after the addition of 8.2 ml of methyl formate, treated with 2.76 g of sodium. The mixture was stirred at room temperature until the reaction was completed and treated with 1N hydrochloric acid while cooling. The organic phase was separated and the aqueous phase was extracted twice with ether. The combined organic phases were washed with saturated sodium chloride solution, dried over sodium sulfate, filtered and evaporated. Distillation yielded methyl 3-hydroxy-2-(α,α,α-trifluoro-m-tolyl)acrylate as a colorless oil of b.p. 59°-62°/0.2 mm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04735940
Source datasetuspto-grants-1988_04
ORD IDord-b4393a48f8994ecca034d8aa17dff6b8
Source noteuspto-grants-1988_04