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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1713884Generated: November 4, 2026

HCID 178453589, compound → HCID 178453586, compound

https://huagongshe.com/reaction/1713884

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178453589HCID 178453589—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
ProductHCID 178453586HCID 17845358692.2%

Reaction Steps

Benzyl [4-(trans-4-{[(tert-butoxycarbonyl)amino]methyl}cyclohexyl)phenyl]carbamate (0.50 g, 1.14 mmol) in EtOH (10 mL) and EtOAc (10 mL) was hydrogenated over 10% Pd/C (100 mg) at ambient pressure and 40° C. After 2 hours the catalyst was removed by filtration and the solution concentrated in vacuo to leave the title compound (320 mg, 86%) as a white solid; 1H NMR δ 0.95-1.02 (2H, m), 1.25-1.39 (12H, m), 1.73-1.75 (4H, m), 2.22-2.25 (1H, m), 2.80 (2H, t), 4.75 (2H, s), 6.46-6.49 (2H, m), 6.78 (1H, t), 6.85 (2H, d)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07795283B2
Source datasetuspto-grants-2010_09
ORD IDord-af30572120e94ce283dbc0f49f174f70
Source noteuspto-grants-2010_09