HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 1-[5-Chloro-8-(2-fluorophenyl)quinolin-7-yl]ethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 1-[5-Chloro-8-(2-fluorophenyl)quinolin-7-yl]ethanone | HCID 67249535 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-[5-Chloro-8-(2-fluorophenyl)quinolin-7-yl]ethanol | HCID 67248433 | — |
Reaction Steps
To a mixture of 1-[5-chloro-8-(2-fluorophenyl)quinolin-7-yl]ethanone (0.032 g, 0.11 mmol) in methanol (0.3 mL) was added sodium tetrahydroborate (0.0040 g, 0.11 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 (33 mg, 100%). LCMS calculated for C17H14ClFNO(M+H)+: m/z=302.1; found: 302.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08680108B2 |
| Source dataset | uspto-grants-2014_03 |
| ORD ID | ord-c7520f0704c043368ae4b9e7e47c048e |
| Source note | uspto-grants-2014_03 |