HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → (2-Chloro-5-methylpyridin-3-yl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2-Chloro-5-methylpyridine-3-carbaldehyde | HCID 9834018 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (2-Chloro-5-methylpyridin-3-yl)methanol | HCID 12056721 | 88% |
Reaction Steps
Sodium borohydride (0.65 g, 0.0167 moles) was added slowly to a well-stirred solution of 2-chloro-5-methylpyridine-3-carbaldehyde (1.3 g, 0.0084 moles) in methanol (20 ml) at 0° C. temperature over a period of 15 minutes. The reaction mass was further stirred for 2 hours at the same temperature. The solvent was removed under reduced pressure and the mass was quenched with water (25 ml). The mass was extracted with ethyl acetate (2×50 ml) and the layers separated. The organic layer was removed under reduced pressure. The residue so obtained was subjected to chromatographic purification on silica gel to give 2-chloro-3-hydroxymethyl-5-methylpyridine as a solid in 88 % yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06566528B1 |
| Source dataset | uspto-grants-2003_05 |
| ORD ID | ord-55e33fcc56a84aee8883be0977b9913f |
| Source note | uspto-grants-2003_05 |