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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 629427Generated: October 30, 2026

Thionyl Chloride → 4-(chloromethyl)-2-fluoro-N-methylbenzamide

https://huagongshe.com/reaction/629427

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantSodium BicarbonateHCID 516892—
Reactant2-fluoro-4-(hydroxymethyl)-N-methylbenzamideHCID 117977065—
SolventTetrahydrofuranHCID 8028—
Product4-(chloromethyl)-2-fluoro-N-methylbenzamideHCID 117977084—

Reaction Steps

To a solution of 2-fluoro-4-(hydroxymethyl)-N-methylbenzamide (2.11 g) in THF (46.1 mL) was added dropwise thionyl chloride (1.01 mL) under ice-cooling, and the mixture was stirred overnight at room temperature. To the reaction solution was added saturated aqueous sodium bicarbonate, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was subjected to silica gel column chromatography (ethyl acetate/hexane). The objective fractions were collected, and washed with diisopropyl ether, and the precipitate was collected by filtration. The filtrate was concentrated, and the residue was washed with diisopropyl ether. This procedure was repeated three times to give the title compound (0.96 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09315458B2
Source datasetuspto-grants-2016_04
ORD IDord-49c2b28852ee465d81d508a1fc4d3447
Source noteuspto-grants-2016_04