HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 18347023, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 18334215 | HCID 18334215 | — |
| Catalyst | Dichloronickel;hexahydrate | HCID 11791229 | — |
| Product | HCID 18347023 | HCID 18347023 | — |
Reaction Steps
Following a similar reaction, separation and purification procedure to that described in Example (59b), 3.96 g of N-[(4-chlorophenyl)-(3-nitrophenyl)methyl]-N-[1-(2,3,4-trifluorophenyl)ethyl]amine [prepared as described in step (a) above], 4.47 g of nickel chloride hexahydrate and 1.42g of sodium borohydride were reacted, to obtain 1.05 g of isomer A and 720 mg, of isomer B of the title compound, each 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-432887d57e89415fb2f04f072d38970e |
| Source note | uspto-grants-2001_12 |