HuagongsheHuagongshe Chemistry Print Report · For research reference only
methyl 4-(N-benzylamino)-1-methyl-1-cyclohexanecarboxylate → Methyl 4-amino-1-methylcyclohexane-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | methyl 4-(N-benzylamino)-1-methyl-1-cyclohexanecarboxylate | HCID 19004646 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 4-amino-1-methylcyclohexane-1-carboxylate | HCID 19004747 | 68.9% |
Reaction Steps
0.2 g of 10% palladium-carbon was added to a solution of 3.1 g of methyl 4-(N-benzylamino)-1-methyl-1-cyclohexanecarboxylate (Example 15) in 200 ml of methanol. The solution was reacted at room temperature under normal-pressure hydrogen gas. The reaction was stopped after 20 hours, the catalyst was filtered out, and the solvent was removed in vacuo from the filtrate. As a result, 1.4 g of methyl 4-amino-1-methyl-1-cyclohexanecarboxylate was obtained as a pale yellow oil, which had the following physiochemical properties:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05344845 |
| Source dataset | uspto-grants-1994_09 |
| ORD ID | ord-37c5bdde4edf4dc9b06b67226728faf9 |
| Source note | uspto-grants-1994_09 |