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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1954677Generated: October 27, 2026

Benzyl chloroformate → (2R)-1-((Benzyloxy)carbonyl)piperidine-2-carboxylic acid

https://huagongshe.com/reaction/1954677

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl chloroformateHCID 10387—
ReactantSodium HydroxideHCID 14798—
ReactantPipecolic acid, (+)-HCID 736316—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product(2R)-1-((Benzyloxy)carbonyl)piperidine-2-carboxylic acidHCID 68834695%

Reaction Steps

D-hPro-OH (5.0 g, 38.7 mmol) was dissolved in tetrahydrofuran (100 mL) and water (30 mL). The pH of the solution was adjusted to 9.5 with 2N NaOH and benzyl chloroformate (5.5 mL, 38.7 mmol) was added dropwise and the pH maintained at 9.5 with 2N NaOH. The reaction was stirred for an additional 1 hour at room temperature. The organic solvent was evaporated in vacuo, and diethyl ether (100 mL) and water (50 mL) were added to the residue. The aqueous layer was separated, the pH of the aqueous solution was adjusted to 2.8 with 3N HCl, and ethyl acetate (150 mL) was added. The organic layer was separated and dried (MgSO4) and the filtrate was concentrated in vacuo to give 9.6 g (95%) of a clear oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06124277
Source datasetuspto-grants-2000_09
ORD IDord-562908c1f98b4860998d2ec81c0eb866
Source noteuspto-grants-2000_09