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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 875623Generated: October 29, 2026

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

https://huagongshe.com/reaction/875623

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 numberUS08981085B2
Source datasetuspto-grants-2015_03
ORD IDord-1cc32ba39e464e699846040a49958179
Source noteuspto-grants-2015_03