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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1292829Generated: October 28, 2026

Chloromethyl Methyl Ether → 3-Acetyl-4-chloromethyl-2,5-dichlorothiophene

https://huagongshe.com/reaction/1292829

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloromethyl Methyl EtherHCID 7864—
Reactant1-(2,5-Dichloro-3-thienyl)ethan-1-oneHCID 118920—
CatalystTitanium TetrachlorideHCID 24193—
SolventDichloromethaneHCID 6344—
Product3-Acetyl-4-chloromethyl-2,5-dichlorothiopheneHCID 17862861266.9%

Reaction Steps

33 ml of titanium tetrachloride (a 2 moles/liter dichloromethane solution, 66.0 mmoles) was dropwise added, at 10° C. with ice-cooling, to a solution of 5.0 g (32;4 mmoles) of 3-acetyl-2,5-dichlorothiophene dissolved in 26 ml (323.0 mmoles) of chloromethyl methyl ether. The mixture was stirred at room temperature for 2 hours to give rise to a reaction. After the completion of the reaction, the reaction action. After the completion of the reaction, the reaction mixture was poured into ice water, followed by extraction with chloroform. The resulting organic layer was washed with sodium bicarbonate, water and an aqueous sodium chloride solution in this order and then dried over anhydrous magnesium sulfate. The resulting solution was subjected to vacuum distillation to remove the solvent contained therein. The residue was purified by silica gel column chromatography (developing solvent: hexane/ethyl acetate=9/1) to obtain 2.6 g (yield: 39.7%) of 3-acetyl-4-chloromethyl-2,5-dichlorothiophene as yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07238689B2
Source datasetuspto-grants-2007_07
ORD IDord-a4dfa32f14554f4fb617f422b4217d64
Source noteuspto-grants-2007_07