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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 471135Generated: October 27, 2026

Hydrochloric Acid → 2-(3-(Hydroxymethyl)phenylthio)ethanol

https://huagongshe.com/reaction/471135

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant(Dimethyl sulfide)trihydroboronHCID 12423031—
Reactant3-(2-(tert-Butyldimethylsilyloxy)ethylthio)benzoic acidHCID 57989336—
SolventTetrahydrofuranHCID 8028—
Product2-(3-(Hydroxymethyl)phenylthio)ethanolHCID 57989304—

Reaction Steps

Borane dimethyl sulfide complex (2M in THF, 17.3 mL) was added dropwise to an ice cold solution of 3-(2-(tert-butyldimethylsilyloxy)ethylthio)benzoic acid (example 65, step a) (2.16 g) in THF (50 mL). The reaction was allowed to warm to RT, then heated at reflux for 2 h. The reaction was cooled in an ice bath and aqueous HCl solution (2M, 50 mL) was added dropwise. The resulting mixture was stirred overnight. The reaction was concentrated to half its original volume and the resulting aqueous extracted with DCM (3×100 mL). The combined organics were washed with brine (100 mL), dried over sodium sulphate, filtered and evaporated. The residue was purified by silica gel chromatography eluting with 4:1 isohexane:ethyl acetate to 100% ethyl acetate gradient. The fractions containing product were combined and evaporated to give the subtitled compound as a clear oil. Yield 0.77 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08629271B2
Source datasetuspto-grants-2014_01
ORD IDord-564738d8d0b34e79ad300bbb867fd015
Source noteuspto-grants-2014_01