HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 70188091, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 70189329 | HCID 70189329 | — |
| Catalyst | Dichloronickel;hexahydrate | HCID 11791229 | — |
| Product | HCID 70188091 | HCID 70188091 | — |
Reaction Steps
Following a procedure similar to that described in Example (59b), 2.06 g of N-[(4-methoxyphenyl)-(3-nitrophenyl)methyl]-N-[(R)-1-phenylethyl]amine [prepared as described in step (a) above], 2.70 g of nickel chloride hexahydrate and 860 mg of sodium borohydride were reacted, separated and purified, to obtain 510 mg of isomer A and 672 mg of isomer B of the title compound, each as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06329405B1 |
| Source dataset | uspto-grants-2001_12 |
| ORD ID | ord-f1ef6d889b0e45269beb4e8b843b7f54 |
| Source note | uspto-grants-2001_12 |