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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2178169Generated: October 30, 2026

Ammonium formate → HCID 89893894, compound

https://huagongshe.com/reaction/2178169

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
ReactantHCID 89894078HCID 89894078—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 89893894HCID 8989389462%

Reaction Steps

To a suspension of (R)-tert-butyl-5-(benzyloxymethyl)-2-oxooxazolidin-3-ylcarbamate (1.908 g, 5.92 mmol) and 10% Pd/C (315 mg, 0.296 mmol) in ethanol (25 mL), ammonium formate (933 mg, 14.80 mmol) was added and the reaction was refluxed, under nitrogen, while stirring for 3 h 30 min. The catalyst was filtered away and the solvent evaporated. The residue was triturated with diisopropyl ether:MeOH=10:1. The title compound was obtained as a white solid (852 mg, 3.67 mmol). Yield=62%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067927B2
Source datasetuspto-grants-2015_06
ORD IDord-8821f51d49b949e2ba80712d98bc3c1c
Source noteuspto-grants-2015_06