HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → [(1-Nitrocyclohexyl)methyl]benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Nitrocyclohexane | HCID 14285 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Product | [(1-Nitrocyclohexyl)methyl]benzene | HCID 4560895 | — |
Reaction Steps
Nitrocyclohexane and benzylbromide are subjected to condensation reaction in the presence of sodium hydride to obtain 1-benzyl-1-nitrocyclohexane. The product is reduced with lithium aluminum hydride to obtain 1-benzyl-1-aminocyclohexane. The product is reacted with methyl chloroformate to obtain 1-benzyl-1-methoxycarbonylaminocyclohexane, and the product is subjected to intramolecular cyclization in the presence of phosphorous oxychloride to obtain spiro[1,2,3,4-tetrahydroisoquinoline-2,1'-cyclohexan]-1-one.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05442055 |
| Source dataset | uspto-grants-1995_08 |
| ORD ID | ord-53c51a70f4434a8692682b441bad0b09 |
| Source note | uspto-grants-1995_08 |