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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 726654Generated: October 25, 2026

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

https://huagongshe.com/reaction/726654

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 sodium hydroxide and benzyl chloroformate (5.5 mL, 38.7 mmol) was added dropwise and the pH maintained at 9.5 with 2N sodium hydroxide. The reaction was stirred for an additional 1 hour at room temperature. The organic solvent was evaporated in vacuo, diethyl ether (100 mL) and water (50 mL) was added to the residue. The aqueous layer separated, the pH of the solution was adjusted to 2.8 with 3N hydrochloric acid and ethyl acetate (150 mL) was added. The organic layer was separated and dried (MgSO4); 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 numberUS05710130
Source datasetuspto-grants-1998_01
ORD IDord-e0b0eabec1134cad9b0eb027b09b8d26
Source noteuspto-grants-1998_01