HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 70188144, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 70189816 | HCID 70189816 | — |
| Catalyst | Dichloronickel;hexahydrate | HCID 11791229 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 70188144 | HCID 70188144 | — |
Reaction Steps
In a similar manner to that described in Example (1b), a solution of N-[(3-nitrophenyl)-(4-methoxyphenyl)methyl]-[(R)-1-(3,4-difluorophenyl)ethyl]amine (1.27 g) [prepared as described in step (a) above] in methanol (50 ml), nickel chloride hexahydrate (1.52 g) and sodium borohydride (510 mg) were reacted, and the reaction mixture was purified by chromatography through a silica gel column using a 1:8 by volume mixture of ethynyl acetate and toluene as the eluant, to afford isomer A (235 mg,) as a yellow oil and isomer B (240 mg) as a pale yellow oil of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06329405B1 |
| Source dataset | uspto-grants-2001_12 |
| ORD ID | ord-428a7a8cc8f74b27a8fc12dbb1e710d8 |
| Source note | uspto-grants-2001_12 |