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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1922596Generated: October 31, 2026

Triethylamine → 1-(Tert-butoxycarbonylamino)propan-2-yl methanesulfonate

https://huagongshe.com/reaction/1922596

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactanttert-butyl N-(2-hydroxypropyl)carbamateHCID 9920508—
SolventDichloromethaneHCID 6344—
Product1-(Tert-butoxycarbonylamino)propan-2-yl methanesulfonateHCID 2313407194.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of tert-butyl 2-hydroxypropylcarbamate (14.3 g, 81.7 mmol) and Et3N (35.6 ml, 245.1 mmol) in CH2Cl2 (250 mL) at 0° C. was slowly added a solution of methanesulfonyl chloride (9.5 mL, 122.6 mmol) in CH2Cl2 (250 mL). The mixture was stirred at 0° C. for 2 h, diluted with CH2Cl2 (300 mL) and washed with water, 1 N HCl, 5% NaHCO3 and brine. The organic layer was dried over MgSO4 and concentrated under reduced pressure to afford 1-(tert-butoxycarbonylamino)propan-2-yl methanesulfonate (19.5 g, 94%) as a light yellow oil. Mass calculated for C9H19NO5S=253.32; found: [M+H]+=254.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173831B2
Source datasetuspto-grants-2012_05
ORD IDord-cff6418b81594b38a831b8c08f5abf47
Source noteuspto-grants-2012_05