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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 746604Generated: October 29, 2026

Methanesulfonyl chloride → HCID 86602659, compound

https://huagongshe.com/reaction/746604

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 58591564HCID 58591564—
SolventDichloromethaneHCID 6344—
ProductHCID 86602659HCID 86602659—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a cooled (0° C.) solution of 2-(6-methyl-benzo[b]thiophen-2-yl)-ethanol (3.22 g, 16.8) mmol) in dichloromethane (100 mL), methanesulfonylchloride (1.56 mL, 20.1 mmol) and DIEA (5.96 mL, 33.5 mmol) were added. The mixture was stirred for 15 min at 0° C. and then allowed to reach room temperature and stirred for an additional 2.5 hrs. It was washed with sat. NaHCO3 (2×) and brine (1×), dried (Na2SO4), filtered and concentrated in vacuo. Methanesulfonic acid 2-(6-methyl-benzo[b]thiophen-2-yl)-ethyl ester was obtained as a solid and used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07393865B2
Source datasetuspto-grants-2008_07
ORD IDord-1ccd6ca2908c48ecaba5009e727bd98f
Source noteuspto-grants-2008_07