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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2248388Generated: October 30, 2026

Water → Benzyl 4-Hydroxy-1-piperidinecarboxylate

https://huagongshe.com/reaction/2248388

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzyl chloroformateHCID 10387—
ReactantPiperidin-4-olHCID 79341—
ReactantDiisopropylethylamineHCID 81531—
SolventDichloromethaneHCID 6344—
ProductBenzyl 4-Hydroxy-1-piperidinecarboxylateHCID 2794620—

Reaction Steps

4-Hydroxypiperidine (10 g., 0.099 mole) and N,N-diisopropylethylamine (87 ml., 0.495 mole) were dissolved in methylene dichloride (200 ml.). The solution was cooled (ice bath) and protected from atmospheric moisture (drying tube), and benzyl chloroformate (14.1 ml., 16.9 g., 0.099 mole) was added over 2 hrs. Water (20 ml.) was added and the solvents were evaporated in vacuo (approx. 1 mm. pressure, solid CO2 cold finger condenser). The residue was shaken together with water (200 ml.) and ethyl acetate (200 ml.), and the mixture was separated. The organic phase was washed with water (4×50 ml.), dried (Na2SO4), and the solvent evaporated to give 1-benzyloxycarbonyl-4-hydroxypiperidine as a colourless oil, I.R.μmax 3800 cm.-1 and 1685cm.-1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05039710
Source datasetuspto-grants-1991_08
ORD IDord-b0b63d5470a349349bc9e5b242e15e60
Source noteuspto-grants-1991_08