HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → (3-(Benzyloxy)pyridin-2-yl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 3-Hydroxypyridine-2-methanol | HCID 84169 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (3-(Benzyloxy)pyridin-2-yl)methanol | HCID 13217540 | 65% |
Reaction Steps
To a solution of 3-hydroxy-2-(hydroxymethyl)pyridine (10.00 g) and KOH (7.00 g) in anhydrous EtOH was added benzyl bromide (7.30 mL) at room temperature under stirring. The reaction mixture was heated to reflux for 24 h, then cooled to rt and filtered. The filtrate was concentrated in vacuo and the residue was chromatographed with a silica gel column (eluting agent: 20:1 (v/v) DCM/MeOH) to give the title compound as a pale yellow solid (7.50 g, 65.00%), HPLC: 95.00%. The compound was characterized by the following spectroscopic data: MS (ESI, pos. ion) m/z: 216.4 (M+1); 1H NMR (400 MHz, CDCl3) δ: 4.39 (br s, 1H), 4.82 (s, 2H), 5.11 (s, 2H), 7.16-7.17 (m, 2H), 7.34-7.40 (m, 5H), 8.15-8.17 (m, 1H) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09181277B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-7452e675d20641e6b0762bc342aefbf1 |
| Source note | uspto-grants-2015_11 |