HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 18347071, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 18334113 | HCID 18334113 | — |
| Catalyst | Dichloronickel;hexahydrate | HCID 11791229 | — |
| Product | HCID 18347071 | HCID 18347071 | — |
Reaction Steps
Following a similar reaction, separation and purification procedure to that described in Example (59b), 3.42 g of N-[1-(3,4-difluorophenyl)ethyl]-N-[(4-fluorophenyl)-(3,4-dimethoxy-5-nitrophenyl)methyl]amine [prepared as described in step (a) above], 3.65 g of nickel chloride hexahydrate and 1.17 g of sodium borohydride were reacted, to obtain 1.10 g of isomer A and 1.39 g of isomer B of the title compound as pale yellow oils, respectively.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06329405B1 |
| Source dataset | uspto-grants-2001_12 |
| ORD ID | ord-103e2c133a9e4174820c73e9c4ddff82 |
| Source note | uspto-grants-2001_12 |