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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1822468Generated: November 2, 2026

Methanesulfonyl chloride → HCID 10379776, compound

https://huagongshe.com/reaction/1822468

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantDiisopropylethylamineHCID 81531—
ReactantBoc-L-leucinolHCID 7018766—
SolventDichloromethaneHCID 6344—
ProductHCID 10379776HCID 10379776—

Reaction Steps

To a solution of ((1S)-1-hydroxymethyl-3-methyl-butyl)-carbamic acid tert-butyl ester (25 g, 115 mmol) in dichloromethane (500 ml) cooled by an ice-water bath was successively added diisopropylethylamine (35.7 g, 276 mmol) and methanesulphonyl chloride (15.81 g, 138 mmol). The resulting solution was stirred over night during which time the mixture was allowed to gradually warm up to ambient temperature. The mixture was washed successively with water, 10% citric acid (aq), water and saturated NaHCO3 (aq), then dried with Na2SO4 and concentrated to a brown solid (32.6 g, 96%) which was used in the next reaction without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07608590B2
Source datasetuspto-grants-2009_10
ORD IDord-4e5f09e6c67043dda0ea480e259d6860
Source noteuspto-grants-2009_10