HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 466874Generated: October 26, 2026
Benzyl chloroformate → N-4-Boc-N-1-Cbz-2-piperazine carboxylic acid
https://huagongshe.com/reaction/466874
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | 4-[(Tert-butoxy)carbonyl]piperazine-2-carboxylic acid | HCID 5175855 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | N-4-Boc-N-1-Cbz-2-piperazine carboxylic acid | HCID 2756777 | 37.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05157041 |
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| Source dataset | uspto-grants-1992_10 |
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| ORD ID | ord-121842e20f2a43e884fb7e53da548441 |
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| Source note | uspto-grants-1992_10 |
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