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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1531231Generated: October 26, 2026

4-Fluorobiphenyl → 4-Fluorobiphenylsulfonyl Chloride

https://huagongshe.com/reaction/1531231

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-FluorobiphenylHCID 9461—
ReactantChlorosulfonic acidHCID 24638—
Product4-Fluorobiphenylsulfonyl ChlorideHCID 18324021—

Reaction Steps

Chlorosulfonic acid (8.7 mL, 0.13 mole) was added dropwise to 4-fluorobiphenyl (10.2 grams, 59 mmol) while stirring in an ice bath. Stirring was continued with ice cooling for 0.5 hours and then the reaction mixture was poured onto ice. The resulting white precipitate was collected by filtration and dissolved in chloroform. The chloroform solution was washed with water and brine, dried over magnesium sulfate and concentrated to afford a white solid. The desired product, 4-fluorobiphenylsulfonyl chloride (4.3 grams, 27%), was separated from 4-fluorobiphenylsulfonic acid (an unwanted side product) by crystallization of the latter from ethyl acetate and crystallization of the remaining material from hexane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06197810B1
Source datasetuspto-grants-2001_03
ORD IDord-30307af61b604ce9be93b965f12d99d0
Source noteuspto-grants-2001_03