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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 267158Generated: October 29, 2026

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

https://huagongshe.com/reaction/267158

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 numberUS05652369
Source datasetuspto-grants-1997_07
ORD IDord-d3f645623a8043029dd84717dd3cf1b7
Source noteuspto-grants-1997_07