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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 337230Generated: October 30, 2026

Methanesulfonyl chloride → HCID 86674089, compound

https://huagongshe.com/reaction/337230

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 64793016HCID 64793016—
SolventDichloromethaneHCID 6344—
ProductHCID 86674089HCID 8667408989.1%

Reaction Steps

Diisopropylethylamine (0.19 ml, 1.17 mmol) was added to a cool (0° C.) solution of (4-Hydroxymethyl-phenyl)-carbamic acid benzyl ester (0.25 g, 0.97 mmol) in DCM (8 ml) and the reaction stirred at this temperature for 5 minutes. After this time, methane sulfonyl chloride (0.09 ml, 1.07 mmol) was added dropwise and the mixture was allowed to warm to room temperature and stirred for 1 hour. The reaction mixture was then diluted with DCM (20 ml) and washed sequentially with saturated sodium bicarbonate solution (10 ml), saturated ammonium chloride (10 ml) and brine (10 ml). The organic layer was separated, dried (MgSO4), filtered and concentrated to afford the title compound (0.29 g, 89% yield) as a yellow oil which was taken forward without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889716B2
Source datasetuspto-grants-2014_11
ORD IDord-3a55568aabed4e3390eb1e20ccdc0448
Source noteuspto-grants-2014_11