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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1255046Generated: October 27, 2026

Methanesulfonyl chloride → Ethyl 2-(methylsulfonyloxy)-2-(thiophen-2-yl)acetate

https://huagongshe.com/reaction/1255046

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantDiisopropylethylamineHCID 81531—
ReactantEthyl 2-hydroxy-2-(thiophen-2-yl)acetateHCID 12266229—
SolventDichloromethaneHCID 6344—
ProductEthyl 2-(methylsulfonyloxy)-2-(thiophen-2-yl)acetateHCID 58556972—

Reaction Conditions

Temperature0 °C

Reaction Steps

Hydroxy-thiophen-2-yl-acetic acid ethyl ester (4.58 g, 24.6 mmol) is dissolved in dry DCM (125 mL) and cooled at 0° C. DIPEA (5.15 mL, 29.5 mmol) and methanesulphonyl chloride (2.11 mL, 27.1 mmol) are added and the resulting solution is stirred at RT for 1 hour. DIPEA (0.859 ml, 4.92 mmol) and methanesulphonyl chloride (0.19 mL, 2.46 mmol) are added again. After being stirred at room temperature for 1 additional hour, a third portion of DIPEA (0.43 mL, 2.46 mmol) and methanesulphonyl chloride (77 ul, 0.98 mmol) is added. After 1 hour the reaction is completed. The mixture is diluted with DCM, washed with sat. NaHCO3, water and brine, dried (Na2SO4), filtered and evaporated. The resulting yellow oil is used in the next step without any further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08455646B2
Source datasetuspto-grants-2013_06
ORD IDord-c412baf9c9634e81a981103a7f0ffa3d
Source noteuspto-grants-2013_06