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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 497288Generated: October 29, 2026

Thioanisole → 2-(4-Bromophenyl)-1-[4-(methylthio)phenyl]ethanone

https://huagongshe.com/reaction/497288

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThioanisoleHCID 7520—
ReactantBenzeneacetic acid, 4-bromo-HCID 74654—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventDiethyl EtherHCID 3283—
SolventThionyl ChlorideHCID 24386—
Product2-(4-Bromophenyl)-1-[4-(methylthio)phenyl]ethanoneHCID 1145006752.3%

Reaction Conditions

Temperature90 °C

Reaction Steps

4-Bromophenylacetic acid (10.8 g, 0.050 mol) was disolved in thionyl chloride (50 mL) and stirred for 30 min at 90° C. The mixture was concentrated and the residual oil was disolved in carbon disulfide (100 mL) and thioanisole (12.5 g, 0.10 mol) was added and the mixture was cooled to 0° C. and AlCl3 (14.7 g, 0.11 mol) was added portionwise. The mixture was stirred at room temperature for 16 h. The resultant dark green suspension was poured into ice water (150 mL) and extracted with CH2Cl2 (150 mL×2), washed with aqueous saturated NaHCO3 (50 mL), dried over MgSO4, and concentrated in vacuo gave the solid. The solid was suspended in ether and collected by filtration to give the title compound (8.4 g, 46%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06949536B2
Source datasetuspto-grants-2005_09
ORD IDord-27033eb6f8eb4fa49fd9598ab91f58ea
Source noteuspto-grants-2005_09