Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2167000Generated: November 2, 2026

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

https://huagongshe.com/reaction/2167000

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 numberUS09044389B2
Source datasetuspto-grants-2015_06
ORD IDord-d2f9cb7a63364c3f9e7b49c29581e913
Source noteuspto-grants-2015_06