HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 70189772, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 70188156 | HCID 70188156 | — |
| Catalyst | Dichloronickel;hexahydrate | HCID 11791229 | — |
| Product | HCID 70189772 | HCID 70189772 | 9.1% |
Reaction Steps
In a similar manner to that described in Example (15b), N-[(3-nitrophenyl)-2-thienylmethyl]-N-[(S)-1-phenylethyl]amine (4.56 g) [prepared as described in step (a) above], nickel chloride hexahydrate (6.42 g) and sodium borohydride (2.04 g) were reacted and purified, to afford isomer A of the title compound (936 mg) as a pale yellow oil and isomer B of the title compound (380 mg) 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-952d9d565bab4cb08fdf49a42eb1818e |
| Source note | uspto-grants-2001_12 |