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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 276203Generated: October 27, 2026

Sodium Hydroxide → (E)-3-cyclohexyl-2-(3,4-difluoro-phenyl)-acrylic acid

https://huagongshe.com/reaction/276203

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant(E)-3-cyclohexyl 2-(3,4-difluoro-phenyl)-acrylic acid methyl esterHCID 67483195—
SolventEthanolHCID 702—
Product(E)-3-cyclohexyl-2-(3,4-difluoro-phenyl)-acrylic acidHCID 6748289197.2%

Reaction Conditions

Temperature40 °C

Reaction Steps

A solution of (E)-3-cyclohexyl 2-(3,4-difluoro-phenyl)-acrylic acid methyl ester (0.55 g, 1.97 mmol) in ethanol (10 mL) was treated with a 1N aqueous sodium hydroxide solution (4 mL). The solution was heated at 40° C. For 15 h, at which time, thin layer chromatography analysis of the mixture indicated the absence of starting material. The reaction mixture was then concentrated in vacuo to remove ethanol, and the residue was diluted with water (30 mL) and then acidified with a 1N aqueous hydrochloric acid solution. The resulting acid was extracted into ethyl acetate (2×30 mL). The combined organic layers were washed with a saturated aqueous sodium chloride solution (1×50 mL), dried over anhydrous magnesium sulfate, filtered, and concentrated in vacuo to afford (E)-3-cyclohexyl-2-(3,4-difluoro-phenyl)-acrylic acid (0.51 g, 97%) as a white solid: mp 119-121° C.; EI-HRMS m/e calcd for C15H16F2O2 (M+H)+267.1196, found 267.1200.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06353111B1
Source datasetuspto-grants-2002_03
ORD IDord-d251a2bb00ec4a0ca4445000138126bd
Source noteuspto-grants-2002_03