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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 77013Generated: October 27, 2026

Methanesulfonyl chloride → HCID 58556972, compound

https://huagongshe.com/reaction/77013

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantDiisopropylethylamineHCID 81531—
ReactantEthyl 2-hydroxy-2-(thiophen-2-yl)acetateHCID 12266229—
SolventDichloromethaneHCID 6344—
ProductHCID 58556972HCID 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 numberUS08835682B2
Source datasetuspto-grants-2014_09
ORD IDord-67f413e2266c48ca9c1cd927e26a83b1
Source noteuspto-grants-2014_09