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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 47645Generated: October 29, 2026

Hydrochloric Acid → (3,5-Difluoro-4-(methylthio)phenyl)methanol

https://huagongshe.com/reaction/47645

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantSodium borohydrideHCID 4311764—
Reactant3,5-Difluoro-4-(methylthio)benzaldehydeHCID 22746682—
SolventTetrahydrofuranHCID 8028—
Product(3,5-Difluoro-4-(methylthio)phenyl)methanolHCID 2274603378.5%

Reaction Steps

To a solution of 3,5-difluoro-4-(methylthio)-benzaldehyde (31.3 g, 0.166 mol) in anhydrous THF (200 mL) cooled with a cold water bath was added sodium borohydride (1.6 g, 0.042 mol) in portions over 30 minutes. After stirring 1 hour at room temperature, excess dilute HCl was added, until gas evolution ceased. Water (600 mL) was added and the mixture extracted with dichloromethane (1×500 mL, 1×100 mL). The combined extracts were washed once with water, dried with magnesium sulfate, and concentrated. Purification by silica gel chromatography using 3% ethyl acetate/10% dichloromethane in hexanes initially, and eluting product with 60% ethyl acetate in hexanes gave [3,5-difluoro-4-(methylthio)-phenyl]methanol as a light yellow liquid (24.8 g, 78%). 1H NMR (CDCl3/400 MHz) 6.88-6.93 (m, 2H), 4.65 (s, 2H), 2.42 (s, 3H). HRMS m/z 190.0266 (M+H+, calcd 190.0264).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06699884B2
Source datasetuspto-grants-2004_03
ORD IDord-d39e4c47ef9b46cbad4614e5f3e8987e
Source noteuspto-grants-2004_03