HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Alcohol → 5-Benzyloxy-2-bromoisonicotinic acid ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 46311464 | HCID 46311464 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-Benzyloxy-2-bromoisonicotinic acid ethyl ester | HCID 86645166 | 61.1% |
Reaction Steps
To a solution of benzylalcohol (1.5 g) in tetrahydrofuran (30 mL) was added sodium hydride (55%, 0.3 g) under ice cooling, and this mixture was stirred at same temperature for 5 minutes. To this reaction mixture was added a solution of 2-bromo-5-fluoroisonicotinic acid ethyl ester (2.9 g) in tetrahydrofuran (30 mL), and this mixture was stirred at room temperature for 2 hours. This reaction mixture was poured into water, and this mixture was extracted with ethyl acetate. This organic layer was washed with water and brine, dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure. The residue was purified by column chromatography on silica gel (eluent: ethyl acetate/n-hexane) to give the title compound (2.4 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09023882B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-bf0d40ada5fa4aa89b056549407ce9fc |
| Source note | uspto-grants-2015_05 |