HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Bicarbonate → (6-Bromonaphthalen-2-yl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-Bromo-6-methoxycarbonylnaphthalene | HCID 854134 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (6-Bromonaphthalen-2-yl)methanol | HCID 13473070 | 96% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
Methyl 6-bromo-2-naphthoate (5 g, 18.9 mmol) was dissolved in purified THF (100 mL) under a nitrogen atmosphere, the reaction solution was cooled down to 0° C., and then diisobutyl aluminum hydride (18.9 mL, 1.0M hexane solution) was added thereto. The reaction mixture solution was stirred at room temperature for 3 hours. Sodium bicarbonate (20 mL) was added to the reaction mixture solution, and then the solvent was removed by extraction with water and dichloromethane. The extracted material was dried in vacuum to thereby obtain a white solid (4.3 g, yield: 95%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08476474B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-b1571d08fcfd4e0289b13b9841a2c7e7 |
| Source note | uspto-grants-2013_07 |