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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 726850Generated: October 26, 2026

Hydrochloric Acid → 3-Difluoromethoxy-2-(o-tolyl)acrylic acid methyl ester

https://huagongshe.com/reaction/726850

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantChlorodifluoromethaneHCID 6372—
ReactantSodium HydroxideHCID 14798—
Reactant15-Crown-5HCID 36336—
ReactantSodiumHCID 5360545—
ReactantMethyl 2-(2-methyl phenyl)-3-hydroxy-2-propenoateHCID 67027340—
SolventWaterHCID 962—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product3-Difluoromethoxy-2-(o-tolyl)acrylic acid methyl esterHCID 53849144—

Reaction Conditions

Temperature5 °C

Reaction Steps

Preparation of ##STR8## 7.76 g of the sodium salt of 3-hydroxy-2-(o-tolyl)-acrylic acid methyl ester and 0.3 g of 15-crown-5 in 160 ml of N-methyl-2-pyrrolidone (NMP) are cooled to 5° C. with stirring. Chlorodifluoromethane is then passed in while simultaneously adding dropwise a solution of 8.5 g of sodium hydroxide in 9.3 ml of water and the reaction mixture is left to react with vigorous stirring at 5°-8° C. for 2 hours. 82 ml of 2N hydrochloric acid are then added dropwise at 0°-8° C. and the phases are separated. The aqueous phase is extracted exhaustively with ethyl acetate and the combined organic phases are washed with a saturated sodium chloride solution. After drying over sodium sulfate, the residue is filtered and concentrated to dryness by evaporation in vacuo. 3-difluoromethoxy-2-(o-tolyl)acrylic acid methyl ester is obtained in the form of a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05710314
Source datasetuspto-grants-1998_01
ORD IDord-99071d58d85a48c1917e9a38df6e2781
Source noteuspto-grants-1998_01