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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1076Generated: October 26, 2026

Triethylamine → Benzyl piperidine-1-carboxylate

https://huagongshe.com/reaction/1076

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBenzyl chloroformateHCID 10387—
ReactantPiperidin-4-olHCID 79341—
ReactantChloroform methanolHCID 21584188—
SolventDichloromethaneHCID 6344—
ProductBenzyl piperidine-1-carboxylateHCID 22874959.2%

Reaction Steps

4-Hydroxypiperidine (10.8 g, 107 mmol) and Et3N (17 mL, 123 mmol) in 80 mL of CH2Cl2 was cooled in an ice bath whereupon benzyl chloroformate (16.3 mL, 114 mmol) was added. After stirring 1.5 h at R.T. the mixture was subjected to standard work-up conditions to give 13.9 g (55%) of N-Cbz-piperidine after chromatography (CHCl3 /MeOH; 10:1). [1H]-NMR(CDCl3) consistent with structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05723490
Source datasetuspto-grants-1998_03
ORD IDord-554bd9dd465641989667d60605d8d5a8
Source noteuspto-grants-1998_03