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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1838503Generated: October 31, 2026

Hydrochloric Acid → 5-(Chloromethyl)-1,3-difluoro-2-(methylthio)benzene

https://huagongshe.com/reaction/1838503

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantDiisopropylethylamineHCID 81531—
Reactant(3,5-Difluoro-4-(methylthio)phenyl)methanolHCID 22746033—
SolventDichloromethaneHCID 6344—
Product5-(Chloromethyl)-1,3-difluoro-2-(methylthio)benzeneHCID 2274574095%

Reaction Steps

To a solution of [3,5-difluoro-4-(methylthio)-phenyl]-methanol (24.0 g, 0.126 mol) in dichloromethane (300 mL) cooled in an ice bath was added methanesulfonylchloride (16.9 g, 0.147 mol) in portions followed by diisopropyl-ethylamine in portions. The mixture was allowed to warm to room temperature, and stirred for 18 hours. 4-dimethyl-aminopyridine was added and the mixture was heated to reflux for 2 hours, cooled, and stirred at room temperature for 18 hours. The mixture was poured into dilute HCl and extracted with dichloromethane once (75 mL) after separating. The combined extracts were washed with dilute sodium chloride, dried using magnesium sulfate, and concentrated. Purification by silica gel chromatography using 5% ethyl acetate in hexanes gave 5-(chloromethyl)-1,3-difluoro-2-(methylthio)benzene as a clear colorless liquid (24.9 g, 95%). 1H NMR (CDCl3/400 MHz) 6.92-6.96 (m, 2H), 4.49 (s, 2H), 2.44 (s, 3H). HRMS m/z 207.9893 (M+, calcd 207.9925).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06673818B2
Source datasetuspto-grants-2004_01
ORD IDord-c652844a480b4fb4a1e392d8c923a93d
Source noteuspto-grants-2004_01