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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 267144Generated: October 25, 2026

Benzyl chloroformate → N-4-Boc-N-1-Cbz-2-piperazine carboxylic acid

https://huagongshe.com/reaction/267144

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl chloroformateHCID 10387—
Reactant4-[(Tert-butoxy)carbonyl]piperazine-2-carboxylic acidHCID 5175855—
SolventSodium HydroxideHCID 14798—
ProductN-4-Boc-N-1-Cbz-2-piperazine carboxylic acidHCID 275677737.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

0.1 g of 4-(tert.butoxycarbonyl)-piperazine- 2-carboxylic acid was dissolved in 10 ml of 1N sodium hydroxide solution, cooled to 0° C. and treated with 0.2 g of benzyl chloroformate. The mixture was allowed to warm to room temperature and was then stirred overnight. The mixture was extracted with diethyl ether. The aqueous phase was then acidified to pH 4 with 2M hydrochloric acid and extracted with ethyl acetate to give 0.06 g of 1-(benzyloxycarbonyl)-4-(tert.butoxycarbonyl)-2-piperazinecarboxylic acid as a white solid; MS: m/e 365 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05652369
Source datasetuspto-grants-1997_07
ORD IDord-18a9fd22300a48d3abd4cf83939a05ec
Source noteuspto-grants-1997_07