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
Participants
| Role | Name | HCID | Charge |
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| Reactant | tert-butyl (1S,2S,4S)-4-(dibenzylamino)-2-methylcyclohexylcarbamate tert-butyl (1R,2R,4R)-4-(dibenzylamino)-2-methylcyclohexylcarbamate | HCID 86650621 | — |
| Catalyst | Palladium hydroxide | HCID 9942167 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | tert-butyl (1S,2S,4S)-4-amino-2-methylcyclohexylcarbamate tert-butyl (1R,2R,4R)-4-amino-2-methylcyclohexylcarbamate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08415381B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-f2acfe32f30141b3adcd034e383b37d0 |
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| Source note | uspto-grants-2013_04 |
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