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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 402085Generated: October 26, 2026

Benzyl chloroformate → HCID 58745550, compound

https://huagongshe.com/reaction/402085

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl chloroformateHCID 10387—
ReactantSodium BicarbonateHCID 516892—
Reactantrac-tert-butyl (3R,4R)-4-amino-3-hydroxypiperidine-1-carboxylateHCID 10727458—
SolventDichloromethaneHCID 6344—
ProductHCID 58745550HCID 58745550—

Reaction Conditions

Temperature2.5 °C

Reaction Steps

To a stirred solution of (±)-trans-4-amino-3-hydroxy-piperidine-1-carboxylic acid tert-butyl ester (9.48 mmol, 2.05 g) in a biphasic mixture of DCM (10 mL) and saturated sodium bicarbonate (10 mL) at 0° C. was added benzyl chloroformate (2.0 mL) drop-wise and continued stirring at 0-5° C. for 1 h. The organic layer was separated, and the aqueous layer was extracted with DCM. The combined organic layers were dried, filtered and concentrated under reduced pressure. The residue was purified by flash silica gel column chromatography by eluting with 50% ethyl acetate in hexanes to provide (±)-trans-4-benzyloxycarbonylamino-3-hydroxy-piperidine-1-carboxylic acid tert-butyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08741900B2
Source datasetuspto-grants-2014_06
ORD IDord-c4bfb5e188a34eb5974b7734bba8348b
Source noteuspto-grants-2014_06