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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 416520Generated: October 25, 2026

Triethylamine → HCID 23134071, compound

https://huagongshe.com/reaction/416520

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactanttert-butyl N-(2-hydroxypropyl)carbamateHCID 9920508—
SolventDichloromethaneHCID 6344—
ProductHCID 23134071HCID 23134071—

Reaction Conditions

Temperature0 °C

Reaction Steps

8.24 g (47.0 mmol) (2-Hydroxy-propyl)-carbamic acid tert-butyl ester were dissolved in 100 ml dichloromethane. 7.8 ml (1.2 equiv.) triethylamine were added and the mixture was cooled to 0° C. At that temperature 4.37 ml (1.2 equiv.) methanesulfonyl chloride were added dropwise. The resulting solution was allowed to reach room temperature and stirred for further 4 h. The mixture was diluted with 100 ml dichloromethane and washed sequentially with a 5% KHSO4-solution, water and brine. The organic phase was dried over anhydrous MgSO4 and concentrated under reduced pressure to give methanesulfonic acid 2-tert-butoxycarbonylamino-1-methyl-ethyl ester in crude form as yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08088925B2
Source datasetuspto-grants-2012_01
ORD IDord-449167024039450ea1bd024540009d2a
Source noteuspto-grants-2012_01