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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1841738Generated: November 4, 2026

Boron tribromide → HCID 86583544, compound

https://huagongshe.com/reaction/1841738

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
ReactantHCID 86583545HCID 86583545—
SolventDichloromethaneHCID 6344—
ProductHCID 86583544HCID 86583544—

Reaction Conditions

Temperature0 °C

Reaction Steps

A 1M solution of BBr3 in CH2Cl2 (4.5 ml, 4.5 mmol) was added at −78° C. to a solution of the ethyl (RS)-(4-cyano-phenylamino)-(4-methoxy-3-methylsulphanyl-phenyl)-acetate (320 mg, 0.899 mmol) obtained in Example 167.2 in CH2Cl2 (10 ml). The mixture was stirred at −78° C. for 5 min., at 0° C. for 30 min. and at room temperature for 2 h. Ice-water was added and the mixture was stirred for 10 min. The mixture was extracted with CH2Cl2. The organic phase was dried, filtered and concentrated. The residue was purified by chromatography (SiO2, hexane/EtOAc 2:1). Ethyl (RS)-(4-cyano-phenylamino)-(4-hydroxy-3-methylsulphanyl-phenyl)-acetate was obtained as a colorless oil (198 mg, 64%); MS: 343 ([M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06683215B2
Source datasetuspto-grants-2004_01
ORD IDord-465ca6d049104f90bf1d677179f7c981
Source noteuspto-grants-2004_01