Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1044051Generated: October 27, 2026

Methanesulfonyl chloride → HCID 58556972, compound

https://huagongshe.com/reaction/1044051

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

Ethyl 2-hydroxy-2-(thiophen-2-yl)acetate (I26) (4.58 g, 24.6 mmol) was 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) were added, and the resulting solution was stirred at room temperature for 1 hour. DIPEA (0.86 ml, 4.92 mmol) and methanesulphonyl chloride (0.19 ml, 2.46 mmol) were added again. After 1 additional hour, a third portion of DIPEA (0.43 ml, 2.46 mmol) and methanesulphonyl chloride (77 ul, 0.98 mmol) was added. After 1 hour, the reaction was completed. The mixture was diluted with DCM, washed with sat. NaHCO3, water and brine, dried (Na2SO4), filtered, and evaporated. The resulting oil was used for the next step without any further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08563577B2
Source datasetuspto-grants-2013_10
ORD IDord-8392a2684bb24921b9b4e24feed42829
Source noteuspto-grants-2013_10