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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 390766Generated: October 29, 2026

Acetyl chloride → 1-(5-Bromo-4-methylthiophen-2-yl)ethan-1-one

https://huagongshe.com/reaction/390766

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
Reactant2-Bromo-3-methylthiopheneHCID 84314—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventDichloromethaneHCID 6344—
Product1-(5-Bromo-4-methylthiophen-2-yl)ethan-1-oneHCID 4548035356.6%

Reaction Steps

Acetyl chloride (7.09 g) is added to a suspension of AlCl3 (11.53 g) in dichloromethane (310 ml) at 0° C. After 45 minutes at 0° C., 2-bromo-3-methylthiophene (5.0 g) is added dropwise. After 1 hour at 0° C., the reaction is quenched by added water (100 ml). The mixture is extracted three times with dichloromethane. The organic phases are combined, dried over MgSO4 and concentrated in vacuo. The crude product is purified by chromatography on silica gel (180 g) eluting with a mixture of ethyl acetate and heptane (1:6) to yield 1-{5-bromo-4-methyl-thiophen-2-yl}-ethanone (3.5 g) as a brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08383659B2
Source datasetuspto-grants-2013_02
ORD IDord-daf0d56ba7ee4564af2947309fd02365
Source noteuspto-grants-2013_02