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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1290698Generated: October 31, 2026

Phosphate → 4-(4-Bromophenoxy)benzene-1-sulfonyl chloride

https://huagongshe.com/reaction/1290698

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphateHCID 1061—
ReactantChlorosulfonic acidHCID 24638—
ReactantSulfuryl chlorideHCID 24648—
ReactantHCID 69416353HCID 69416353—
SolventDichloromethaneHCID 6344—
Product4-(4-Bromophenoxy)benzene-1-sulfonyl chlorideHCID 12249741159.9%

Reaction Steps

To a solution of 12.45 g (50 mmol) of 4-bromobiphenyl ether in 50 mL of dichloromethane at -5° C. was added 9.9 mL (17.4 g, 150 mmol) of chlorosulfonic acid dropwise. After the addition was complete, the reaction was allowed to warm to room temperature for one hour (needed to completely convert the initially formed sulfonic acid to the sulfonyl chloride). The reaction mixture was added to cold pH 7 phosphate buffer (ca. 0.5M) and twice extracted with 50 mL of dichloromethane. The organic extracts were combined and washed with brine, dried over sodium sulfate, and concentrated. Addition of hexane to the residual syrup and re-concentration gave 13.9 g (80%) of 4-(4-bromophenoxy)benzenesulfonyl chloride as a white powder: mp 80.9° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05753653
Source datasetuspto-grants-1998_05
ORD IDord-680cb9d273d6457abebe78ba0c2e8453
Source noteuspto-grants-1998_05