HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → (4-(Benzyloxy)-2,6-dimethylphenyl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 4-(Benzyloxy)-2,6-dimethylbenzaldehyde | HCID 11160803 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (4-(Benzyloxy)-2,6-dimethylphenyl)methanol | HCID 67317571 | 97% |
Reaction Steps
Treat a solution of 4-Benzyloxy-2,6-dimethyl-benzaldehyde (6.4 g, 27 mmol) in Methanol (60 mL) with Sodium borohydride (0.82 g, 22 mmol). Stir the reaction for 1 hr at room temperature. Quench the reaction with a saturated solution of sodium bicarbonate in water and extract with Et2O. Wash the organic with brine, dry over MgSO4, and filter. Remove the solvent to afford 6.3 g (97%) of product. 1H NMR (d6-CDCl3) δ 7.31-7.43 (m, 5H), 6.65 (s, 2H), 5.01 (s, 2H), 4.66 (s, 2H), 2.38 (s, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07981918B2 |
| Source dataset | uspto-grants-2011_07 |
| ORD ID | ord-c8738ca60e3e43f6bde34b7a427ade02 |
| Source note | uspto-grants-2011_07 |