HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 70188112, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 70188145 | HCID 70188145 | — |
| Catalyst | Dichloronickel;hexahydrate | HCID 11791229 | — |
| Product | HCID 70188112 | HCID 70188112 | — |
Reaction Steps
Following a similar reaction, separation and purification procedure to that described in Example (59b), 8.32 g of N-[(4-methoxyphenyl)-(3-nitrophenyl)methyl]-N-[(R)-1-(naphthalen-1-yl)ethyl]amine [prepared as described in step (a) above], 9.51 g of nickel chloride hexahydrate and 3.03 g of sodium borohydride were reacted, to obtain 1.15 g of isomer A and 462 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-ca45d4fe14d741b1a9878539cb5be6a7 |
| Source note | uspto-grants-2001_12 |