HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 2-(4-(4-Chloro-3-(trifluoromethyl)phenoxy)phenyl)ethanamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Chloro-4-(4-(2-nitroethyl)phenoxy)-2-(trifluoromethyl)benzene | HCID 67775633 | — |
| Catalyst | Dichloronickel;hexahydrate | HCID 11791229 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-(4-(4-Chloro-3-(trifluoromethyl)phenoxy)phenyl)ethanamine | HCID 67775548 | 57% |
Reaction Steps
To the mixture of 1-chloro-4-(4-(2-nitroethyl)phenoxy)-2-(trifluoromethyl)benzene (17 g, 49.2 mmol) and nickel(II) chloride hexahydrate (46.6 g, 197 mmol) in methanol (300 mL) at 0° C. was added NaBH4 (3.72 g, 98 mmol) portion wise. The reaction mixture was stirred at rt overnight. Purification via a column chromatography afforded the title compound as a yellow oil (8.86 g, 51.4% yield). LCMS: rt=2.51 min, [M+H+]=316.1
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09174968B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-f6e21dbff9c1408aa50675613cc0d20a |
| Source note | uspto-grants-2015_11 |