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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 586612Generated: November 1, 2026

Acetyl chloride → 1-(4-(Methylthio)phenyl)ethan-1-one

https://huagongshe.com/reaction/586612

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantThioanisoleHCID 7520—
ReactantAluminum(III) ChlorideHCID 6451240—
Solvent1,1-DichloroethaneHCID 6365—
Product1-(4-(Methylthio)phenyl)ethan-1-oneHCID 74501—

Reaction Conditions

Temperature0 °C

Reaction Steps

Acetyl chloride (8.2 g, 0.105 mol) is added to a suspension of AlCl3 (16 g, 0.12 mol) in dichloroethane (50 ml) cooled to 0° C.; the mixture is stirred for 15 min and a solution of thioanisole (12.4 g, 0.1 mol) in dichloroethane (20 ml) is then added dropwise; the temperature is kept below 20° C. by cooling (30 min). The mixture is stirred for a further 1 h and allowed to stand at RT overnight. The Lewis acid complex is decomposed by addition of ice water (100 ml) with cooling, the organic phase is separated in a separating funnel, and the aqueous phase is extracted a further 2 times with dichloroethane (100 ml). The combined extracts are dried over Na2SO4 sicc. and concentrated to ¼ of the starting volume. The red-brown residue (15.2 g) is washed with diethyl ether (20 ml) and hexane (20 ml): 12 g of light red (brick-red) substance result.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06936632B2
Source datasetuspto-grants-2005_08
ORD IDord-81864a8930494914b6d7ebd096764e73
Source noteuspto-grants-2005_08