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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2220647Generated: November 1, 2026

Triethylamine → (R)-2-((tert-butoxycarbonyl)amino)propyl methanesulfonate

https://huagongshe.com/reaction/2220647

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactanttert-butyl N-((2R)-1-hydroxypropan-2-yl)carbamateHCID 13200309—
SolventDichloromethaneHCID 6344—
Product(R)-2-((tert-butoxycarbonyl)amino)propyl methanesulfonateHCID 14427185—

Reaction Steps

Methanesulfonyl chloride (0.64 mL) was added dropwise to an ice-cooled mixture of (R)-(+)-2-(tert-butoxycarbonylamino)-propanol (1.31 g) and triethylamine (1.6 mL) in methylene chloride (20 mL) with stirring, and the mixture was stirred at that temperature for 1 hr. The reaction mixture was washed successively with water and brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure to afford the title compound (1.93 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07417169B2
Source datasetuspto-grants-2008_08
ORD IDord-fcaba5752dee4b9ea0c3b341aba2b82f
Source noteuspto-grants-2008_08