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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 54109Generated: October 31, 2026

Water → N2 (benzyloxycarbonyl)-N1-tert.butyl-4(S)-(methanesulphonyloxy)-L-prolinamide

https://huagongshe.com/reaction/54109

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantN2 (benzyloxycarbonyl)-N1-tert.butyl-4(S)-hydroxy-L-prolinamideHCID 86746280—
SolventPyridineHCID 1049—
ProductN2 (benzyloxycarbonyl)-N1-tert.butyl-4(S)-(methanesulphonyloxy)-L-prolinamideHCID 86746278—

Reaction Conditions

Temperature0 °C

Reaction Steps

0.32 g of N2 -(benzyloxycarbonyl)-N1 -tert.butyl-4(S)-hydroxy-L-prolinamide was dissolved in 5 ml of dry pyridine while stirring, cooled to 0° C. and treated dropwise with 0.82 ml of methanesulphonyl chloride. The solution was stirred at 0° C. for a further 2 hours. The mixture was poured into a mixture of ice and water which was then extracted with ethyl acetate. The combined organic extracts were washed with 2M hydrochloric acid and then with saturated sodium bicarbonate solution and subsequently dried over anhydrous sodium sulphate. After evaporation there was obtained 0.5 g of N2 -(benzyloxycarbonyl)-N1 -tert.butyl-4(S)-(methanesulphonyloxy)-L-prolinamide as an oil which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05620987
Source datasetuspto-grants-1997_04
ORD IDord-03538aec98b84714b4513fb8406b1287
Source noteuspto-grants-1997_04