HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 70189275, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 70188089 | HCID 70188089 | — |
| Catalyst | Dichloronickel;hexahydrate | HCID 11791229 | — |
| Product | HCID 70189275 | HCID 70189275 | — |
Reaction Steps
Following a similar reaction, separation and purification procedure to that described in Example (59b), 2.46 g of N-[(4-fluorophenyl)-(3-nitrophenyl)methyl]-N-[(R)-1-(3,4,5-trifluorophenyl)ethyl]amine [prepared as described in step (a) above], 2.90 g of nickel chloride hexahydrate and 927 mg of sodium borohydride were reacted, to obtain 760 mg of isomer A and 716 mg of isomer B of the title compound, each as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06329405B1 |
| Source dataset | uspto-grants-2001_12 |
| ORD ID | ord-2caa0dc9087f44a4b78f33aaa99dbe81 |
| Source note | uspto-grants-2001_12 |