HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → (4-Chloro-6-methylpyridin-2-yl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Ethyl 4-chloro-6-methylpyridine-2-carboxylate | HCID 22727099 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (4-Chloro-6-methylpyridin-2-yl)methanol | HCID 22727138 | 95% |
Reaction Steps
A solution of ethyl 4-chloro-6-methylpyridine-2-carboxylate (0.80 g) in methanol (30 ml) was treated at room temperature portionwise with sodium borohydride (1.51 g) and the reaction mixture was heated under reflux for 2 hours. The reaction mixture was concentrated and the resultant residue was combined with water and ethyl acetate, and the organic phase was isolated, dried and concentrated to obtain the title compound (0.60 g) as a tan powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06723722B1 |
| Source dataset | uspto-grants-2004_04 |
| ORD ID | ord-9fbab4c950f7460da320124c38b87706 |
| Source note | uspto-grants-2004_04 |