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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 270648Generated: October 27, 2026

Dichloromethane → 3-Chloromethyl-2-(2-methanesulfonyloxyethyl) thiophene

https://huagongshe.com/reaction/270648

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-(3-Hydroxymethylthiophen-2-yl)ethanolHCID 11182761—
Product3-Chloromethyl-2-(2-methanesulfonyloxyethyl) thiopheneHCID 8778073391%

Reaction Steps

2.0 g of the compound obtained in Example 2 was dissolved in 35 mL of dichloromethane, and the resulting solution was cooled to below 5° C. To the solution, 3.0 g of methanesulfonyl chloride and 4.1 g of diisopropylethylamine were added, and the resulting mixture was stirred for 30 minutes. 30 mL of dichloromethane was added to the reaction solution, and the resulting mixture was washed twice with 30 mL portions of water. The organic layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure to obtain 2.9 g (yield of 91%) of the title compound as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07449580B2
Source datasetuspto-grants-2008_11
ORD IDord-b85309a0af3f4bfbbe641ef3461e2f8d
Source noteuspto-grants-2008_11