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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2203704Generated: October 31, 2026

Benzyl chloroformate → cis-Tert-butyl 3-(benzyloxycarbonylamino)-4-fluoropiperidine-1-carboxylate

https://huagongshe.com/reaction/2203704

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl chloroformateHCID 10387—
Reactantcis-Tert-butyl 3-azido-4-fluoropiperidine-1-carboxylateHCID 131729718—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
SolventPyridineHCID 1049—
Productcis-Tert-butyl 3-(benzyloxycarbonylamino)-4-fluoropiperidine-1-carboxylateHCID 13172971922%

Reaction Steps

A mixture of cis-tert-butyl 3-azido-4-fluoropiperidine-1-carboxylate (1.40 g, 5.73 mmol) and 10% Pd/C (0.61 g, 0.57 mmol) in MeOH (20 mL) was charged 1 atmosphere H2 and stirred at room temperature for 1 hour. The catalyst was removed by filtration and washed with methanol. The filtrate was concentrated in vacuo. The residue obtained was dissolved in pyridine (10 mL) and benzyl carbonochloridate (1.61 mL, 11.46 mmol) was added. The reaction was stirred at room temperature for 2 hours. The pyridine was removed in vacuo, and the residue was dissolved in ethyl acetate (30 mL), washed with brine, dried (sodium sulfate) and concentrated in vacuo. The residue obtained was purified by flash chromatography on silica gel (hexane:ethyl acetate 3:1) to give cis-tert-butyl 3-(benzyloxycarbonylamino)-4-fluoropiperidine-1-carboxylate (0.44 g, 22%) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365568B2
Source datasetuspto-grants-2016_06
ORD IDord-447b217066244f368799a919f7bff473
Source noteuspto-grants-2016_06