HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 3-{[1-(3,5-Difluorophenyl)ethylamino]-(4-isopropoxyphenyl)methyl}phenylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | N-[1-(3,5-Difluorophenyl)ethyl]-N-[(3-nitrophenyl)-(4-isopropoxyphenyl)methyl]amine | HCID 18334091 | — |
| Catalyst | Dichloronickel;hexahydrate | HCID 11791229 | — |
| Product | 3-{[1-(3,5-Difluorophenyl)ethylamino]-(4-isopropoxyphenyl)methyl}phenylamine | HCID 18334099 | 91.9% |
Reaction Steps
Following a similar procedure to that described in Example (1b), 1.17 g of N-[1-(3,5-difluorophenyl)ethyl]-N-[(3-nitrophenyl)-(4-isopropoxyphenyl)methyl]amine [prepared as described in step (a) above], 1.50 g of nickel chloride hexahydrate and 437 mg of sodium borohydride were reacted, to obtain 1.0 g of the title compound 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-b5a97f5f2d66414fa9ada968c6a31dc3 |
| Source note | uspto-grants-2001_12 |