HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 18334100, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 18334191 | HCID 18334191 | — |
| Catalyst | Dichloronickel;hexahydrate | HCID 11791229 | — |
| Product | HCID 18334100 | HCID 18334100 | — |
Reaction Steps
Following a similar procedure to that described in Example (1b), 660 mg of isomer B of N-[1-(3,4-difluorophenyl)ethyl]-N-[(4-fluorophenyl)-(2-methoxy-5-nitrophenyl)methyl]amine [prepared as described in step (a) above], 762 mg of nickel chloride hexahydrate and 243 mg of sodium borohydride were reacted, to obtain 332 mg of isomer B of the title compound as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06329405B1 |
| Source dataset | uspto-grants-2001_12 |
| ORD ID | ord-026ceb713e73432ab370af957816b327 |
| Source note | uspto-grants-2001_12 |