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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1583285Generated: November 1, 2026

Sulfuryl chloride → 4-(2-Bromo-1,1,2-trifluoroethoxy)-2-chlorophenol

https://huagongshe.com/reaction/1583285

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuryl chlorideHCID 24648—
Reactant4-(2-Bromo-1,1,2-trifluoroethoxy)phenolHCID 13228498—
CatalystDiphenyl sulfideHCID 8766—
SolventAcetic AcidHCID 176—
Product4-(2-Bromo-1,1,2-trifluoroethoxy)-2-chlorophenolHCID 13228501—

Reaction Steps

12.2 g of 4-(2-bromo-1,1,2-trifluoroethoxy)-phenol and 5 drops of diphenyl sulfide were dissolved in 30 ml of glacial acetic acid, and 6.1 g of sulfuryl chloride were added, a little at a time, at 25° C. After 3 hours at 25° C., the volatile components were removed, the residue was taken up with 300 ml of methylene chloride, and the solution was washed with 100 ml of 10% strength NaHCO3 solution and 100 ml of water, dried over Na2SO4 and distilled at 82° C./0.3 mbar. Yield: 12.6 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04551448
Source datasetuspto-grants-1985_11
ORD IDord-d2a3074b604c4089a52010e1c3aefd2c
Source noteuspto-grants-1985_11