HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 18347056, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 18347030 | HCID 18347030 | — |
| Catalyst | Dichloronickel;hexahydrate | HCID 11791229 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 18347056 | HCID 18347056 | — |
Reaction Steps
In a similar manner to that described in Example (1b), a solution of N-[(4-methoxyphenyl)-(3-nitrophenyl)methyl]-N-[2-(cyclohexen-1-yl)ethyl]amine (2.80 g) [prepared as described in step (a) above] in methanol (60 m), nickel chloride hexahydrate (3.61 g) and sodium borohydride (1.15 g) were reacted, to afford a mixture (2.15 g) of the title compound and the reduction product of the title compound, that is 3-[(4-methoxyphenyl)-(2-cyclohexylethylamino)methyl]phenylamine, as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06329405B1 |
| Source dataset | uspto-grants-2001_12 |
| ORD ID | ord-fcc092fc51db4610ac36594b1eb2b740 |
| Source note | uspto-grants-2001_12 |