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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1963909Generated: October 30, 2026

tert-butyl (1S,2S,4S)-4-(dibenzylamino)-2-methylcyclohexylcarbamate tert-butyl (1R,2R,4R)-4-(dibenzylamino)-2-methylcyclohexylcarbamate → tert-butyl (1S,2S,4S)-4-amino-2-methylcyclohexylcarbamate tert-butyl (1R,2R,4R)-4-amino-2-methylcyclohexylcarbamate

https://huagongshe.com/reaction/1963909

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl (1S,2S,4S)-4-(dibenzylamino)-2-methylcyclohexylcarbamate tert-butyl (1R,2R,4R)-4-(dibenzylamino)-2-methylcyclohexylcarbamateHCID 86650621—
CatalystPalladium hydroxideHCID 9942167—
SolventEthanolHCID 702—
Producttert-butyl (1S,2S,4S)-4-amino-2-methylcyclohexylcarbamate tert-butyl (1R,2R,4R)-4-amino-2-methylcyclohexylcarbamateHCID 86650623—

Reaction Steps

A mixture of tert-butyl (1S,2S,4S)-4-(dibenzylamino)-2-methylcyclohexylcarbamate/tert-butyl (1R,2R,4R)-4-(dibenzylamino)-2-methylcyclohexylcarbamate (750 mg, 1.836 mmol) and Pearlman's catalyst (290 mg, 2.73 mmol) in EtOH (35 mL) was hydrogenated in a steel bomb under H2-atmosphere (pressure ˜75 psi) for 16 hr. The steel bomb was flushed with Argon, Celite and methanol were added. The mixture was filtered and concentrated in vacuo. The white resulting residue was dissolved in acetonitrile/water (1:1) and lyophilized giving crude tert-butyl (1S,2S,4S)-4-amino-2-methylcyclohexylcarbamate/tert-butyl (1R,2R,4R)-4-amino-2-methylcyclohexylcarbamate, which was directly used in the next step without further purification. Yield: 412 mg. LCMS (m/z): 173.2/229.3 [M+H]+; Retention time=0.54 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415381B2
Source datasetuspto-grants-2013_04
ORD IDord-f2acfe32f30141b3adcd034e383b37d0
Source noteuspto-grants-2013_04