HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 67246913, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 67248764 | HCID 67248764 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 67246913 | HCID 67246913 | — |
Reaction Steps
To a mixture of 1-[8-(3,5-difluorophenyl)quinolin-7-yl]ethanone (0.057 g, 0.20 mmol) in methanol (0.5 mL) was added sodium tetrahydroborate (0.0076 g, 0.20 mmol). The reaction was stirred at room temperature for 1 hour, quenched with saturated sodium bicarbonate, and extracted with ethyl acetate. The combined organic layers were washed with brine, dried over magnesium sulfate, and then concentrated to dryness under reduced pressure. The resulting residue was used in next step (48 mg, 84.1%). LCMS calculated for C17H14F2NO(M+H)+: m/z=286.1; found: 286.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08680108B2 |
| Source dataset | uspto-grants-2014_03 |
| ORD ID | ord-67ca755629b0456a951d3eee7f243416 |
| Source note | uspto-grants-2014_03 |