HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → (6-o-Tolylpyridin-3-yl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 6-(2-Methylphenyl)pyridine-3-carbaldehyde | HCID 24729662 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (6-o-Tolylpyridin-3-yl)methanol | HCID 24729916 | 100% |
Reaction Steps
To a solution of 1.070 g (5.43 mmol) of 6-o-tolylnicotinaldehyde in 19 mL of ethanol at 0-5° C., was added 287 mg(7.5 mmol, 1.4 eq.) of sodium borohydride. After 2 h, the reaction mixture was quenched with saturated sodium bicarbonate solution and, after 30 min, partitioned between dichloromethane and brine. The organic extract was dried over magnesium sulfate and concentrated to give the indicated product as a colorless oil, 1.08 g, 100% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07534763B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-be46d817115f47078c09952a97e3d274 |
| Source note | uspto-grants-2009_05 |