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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2072302Generated: October 27, 2026

Boron trifluoride etherate → 3-Benzylmercapto-4-carbomethoxy benzyl alcohol

https://huagongshe.com/reaction/2072302

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron trifluoride etherateHCID 8000—
Reactant3-Benzylmercapto-4-carbomethoxy benzoic acidHCID 54108258—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventSodium borohydrideHCID 4311764—
Product3-Benzylmercapto-4-carbomethoxy benzyl alcoholHCID 5440904865.2%

Reaction Steps

28 ml of boron trifluoride etherate is added to a suspension of 46 g of crude 3-benzylmercapto-4-carbomethoxy benzoic acid in 750 ml of anhydrous tetrahydrofuran and 7 g of sodium borohydride. The reaction mixture is stirred for 3-4 hours at room temperature, then diluted with about 20 ml of 2N hydrochloric acid and 500 ml of water. The product obtained is extracted with ether and the ether extract is washed with water and saturated sodium chloride solution, dried over sodium sulfate and evaporated to dryness. Crystallization from ethyl acetate:hexane (1:2) yielded 28.6 g of 3-benzylmercapto-4-carbomethoxy benzyl alcohol having a melting point of 89.5°-92° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04051148
Source datasetuspto-grants-1977_09
ORD IDord-ea52d62c84174c999e6a506d1179c345
Source noteuspto-grants-1977_09