HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → (3-Fluoro-2-methoxyphenyl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 3-Fluoro-2-methoxybenzaldehyde | HCID 12572277 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (3-Fluoro-2-methoxyphenyl)methanol | HCID 22505951 | 87.5% |
Reaction Steps
To a solution of 3-fluoro-2-methoxy-benzaldehyde (3.41 g, 22.1 mmol) in methanol (20 mL) is slowly added portionwise sodium borohydride (1.00 g, 26.6 mmol). The reaction is stirred at room temperature under nitrogen overnight. The reaction is diluted with diethyl ether, washed with water twice, dried over anhydrous sodium sulfate, filtered, and concentrated to afford 3.02 g (87%) of the title compound as a clear colorless oil. 1H NMR (400 MHz, CDCl3) δ 7.09-6.92 (m, 3H), 4.65 (d, 2H), 3.97 (s, 3H), 2.14 (t, 1H, OH).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08486943B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-e7b779f0ee9943a8bb1400187666e2ee |
| Source note | uspto-grants-2013_07 |