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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 270647Generated: October 27, 2026

Dichloromethane → 2-(2-Chloroethyl)-3-chloromethylthiophene

https://huagongshe.com/reaction/270647

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantSulfuryl chlorideHCID 24648—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-(3-Hydroxymethylthiophen-2-yl)ethanolHCID 11182761—
Product2-(2-Chloroethyl)-3-chloromethylthiopheneHCID 6931334527%

Reaction Conditions

Temperature-3 °C

Reaction Steps

3.0 g of the compound obtained in Example 2 was dissolved in 57 mL of dichloromethane, and the resulting solution was cooled to −3° C. To the solution, 6.1 g of diisopropylethylamine and 3.1 g of sulfuryl chloride were added, and the resulting mixture was stirred for 30 min at the same temperature and for an hour at room temperature. 20 mL of dichloromethane was added to the reaction solution, and the resulting mixture was washed twice with 40 mL portions of water. The organic layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was subjected to a silica gel column chromatography (eluent, n-hexane:ethyl acetate=10:1) to obtain 1.0 g (yield of 27%) of the title compound as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07449580B2
Source datasetuspto-grants-2008_11
ORD IDord-3a5d256c0c354ff4930801631dd178db
Source noteuspto-grants-2008_11