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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 741687Generated: October 30, 2026

Thioanisole → 1-(4-(methylthio)phenyl)-2-phenylethanone

https://huagongshe.com/reaction/741687

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThioanisoleHCID 7520—
ReactantPhenylacetyl chlorideHCID 7679—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventChloroformHCID 6212—
Product1-(4-(methylthio)phenyl)-2-phenylethanoneHCID 276008864.4%

Reaction Steps

To a cold (0° C.) solution of phenylacetyl chloride (92.8 g, 0.6 mol) in CHCl3 (1.2 L) was added AlCl3 (80 g, 0.6 mol) in portions. Thioanisole (62.1 g, 0.5 mol) was then added dropwise. The resulting mixture was stirred at r.t. for 1.5 h. The mixture was poured into 4 L of ice and extracted with CHCl3. The combined organic extracts were dried over MgSO4, filtered and concentrated. The residue was slurried in 300 mL of 20 % EtOAc/hexane, filtered and washed with hexane to give 78 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05552422
Source datasetuspto-grants-1996_09
ORD IDord-a6a097ed0fc64b7dbbd0fe62419cbf75
Source noteuspto-grants-1996_09