HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 2',6-Dichloro-4-ethyl-[1,1'-biphenyl]-3-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2',6-Dichloro-4-vinyl-[1,1'-biphenyl]-3-amine | HCID 90460386 | — |
| Catalyst | Cuprous chloride | HCID 62652 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2',6-Dichloro-4-ethyl-[1,1'-biphenyl]-3-amine | HCID 90462567 | 59.4% |
Reaction Steps
A mixture of 2′,6-dichloro-4-vinyl-[1,1′-biphenyl]-3-amine (500 mg, 1.9 mmol), CuCl (225 mg, 2.28 mmol) in MeOH (10 mL) at 0° C., NaBH4 (722 mg, 19 mmol) was added in portions and the resulting mixture was stirred at room temperature for 20 min. The reaction was quenched with water and extracted with ethyl acetate. The organic layer was washed with brine, dried over Na2SO4 and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel (petroleum ether/ethyl acetate=30:1) to afford the desired product (300 mg, 59.4% yield). ESI-MS m/z: 266.0[M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09227978B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-84a01c8671a245809dca9c8cb91b8a6d |
| Source note | uspto-grants-2016_01 |