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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 859889Generated: October 30, 2026

(3R,4S)-3-azidomethyl-1-benzyloxycarbonyl-4-fluoropyrrolidine → benzyl (3S,4S)-3-(aminomethyl)-4-fluoropyrrolidine-1-carboxylate

https://huagongshe.com/reaction/859889

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3R,4S)-3-azidomethyl-1-benzyloxycarbonyl-4-fluoropyrrolidineHCID 86600236—
ReactantHCID 178418361HCID 178418361—
CatalystPlatinum oxide (PtO)HCID 82844—
SolventEthanolHCID 702—
Productbenzyl (3S,4S)-3-(aminomethyl)-4-fluoropyrrolidine-1-carboxylateHCID 6670492092.3%

Reaction Steps

(3R,4S)-3-Azidomethyl-1-benzyloxycarbonyl-4-fluoropyrrolidine (1.35 g) was dissolved in ethanol (30 mL). To this solution, platinum oxide (IV) (190 mg) was added and the mixture was stirred at room temperature for 2 hours in a stream of hydrogen (provided from a balloon). Subsequently, the catalyst was collected from the reaction mixture by filtration through a Celite pad. The collected catalyst and the Celite pad were washed with ethanol. The filtrate and the washing solution were combined and the combined organic layer was concentrated under reduced pressure. The resulting residue was purified on a silica gel column (eluant=ethyl acetate: methanol=10:1) to give 1.13 g of (3S,4S)-3-aminomethyl-1-benzyloxycarbonyl-4-fluoropyrrolidine as a pale brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07153851B2
Source datasetuspto-grants-2006_12
ORD IDord-7b21105f6fb24da4a3e11878c6e0d37c
Source noteuspto-grants-2006_12