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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 325166Generated: October 27, 2026

Benzoyl chloride → Benzoyl fluoride

https://huagongshe.com/reaction/325166

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
Reactant(Bis(2-methoxyethyl)amino)sulfur trifluorideHCID 2734690—
SolventDichloromethaneHCID 6344—
ProductBenzoyl fluorideHCID 6799999.9%

Reaction Steps

A solution of benzoyl chloride (141 mg, 1 mmol) in CH2Cl2 (5.0 mL) was added to bis(methoxyethyl)aminosulfur trifluoride (567 mg, 3.0 mmol ) under N2 and stirred for 16 h at room temperature. After work-up as above benzoyl fluoride (124 mg, quantitative yield) was obtained. The product was identified by g.c.m.s. M+=124

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06222064B1
Source datasetuspto-grants-2001_04
ORD IDord-c698cb0ddf45485f8c3f34cce99c38f2
Source noteuspto-grants-2001_04