Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 9645Generated: October 26, 2026

Hydrochloric Acid → {3-[(Benzylthio)methyl]-5-[4-(trifluoromethyl)phenyl]thien-2-yl}methanol

https://huagongshe.com/reaction/9645

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantAluminium lithium hydrideHCID 21226445—
ReactantEthyl 3-[(benzylthio)methyl]-5-[4-(trifluoromethyl)phenyl]thiophene-2-carboxylateHCID 21986405—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product{3-[(Benzylthio)methyl]-5-[4-(trifluoromethyl)phenyl]thien-2-yl}methanolHCID 21986478—

Reaction Steps

A solution of ethyl 3-[(benzylthio)methyl]-5-[4-(trifluoromethyl)phenyl]thiophene-2-carboxylate (intermediate 45, 0.87 g) in dry tetrahydrofuran (5 ml) was cooled to 0° C. and 1M lithium aluminium hydride solution in diethyl, ether (0.299 ml) added. The reaction mixture as stirred with cooling for 3 hours. Water (0.5 ml) was added drop-wise followed by 2M hydrochloric acid (0.5 ml), the further water (50 ml), the resulting mixture was extracted twice with ethyl acetate, the extracts were combined, dried over magnesium sulfate and concentrated. The residue was purified by SPE (Si cartridge) eluting initially with cyclohexane:chloroform (1:1) and then chloroform to give the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07091237B2
Source datasetuspto-grants-2006_08
ORD IDord-970f584521ce4e678ff7c29f9c38f8c9
Source noteuspto-grants-2006_08