HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 18334248, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 18334143 | HCID 18334143 | — |
| Catalyst | Dichloronickel;hexahydrate | HCID 11791229 | — |
| Product | HCID 18334248 | HCID 18334248 | — |
Reaction Steps
Following, a similar reaction, separation and purification procedure to that described in Example (59b), 3.39 g of N-[1-(3,5-dichlorophenyl)ethyl]-N-[(4-fluorophenyl)-(3-nitrophenyl)methyl]amine [prepared as described in step (a) above], 3.86 g of nickel chloride hexahydrate and 1.23 g of sodium borohydride were reacted, to obtain 970 mg of isomer A and 567 mg of isomer B of the title compound as a pale yellow oil and a white solid, respectively.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06329405B1 |
| Source dataset | uspto-grants-2001_12 |
| ORD ID | ord-d9b50d97596049acb4a9b6192b6b35f9 |
| Source note | uspto-grants-2001_12 |