HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Chloride → (5-Chloro-4-methoxy-6-methylpyridin-3-yl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 58201192 | HCID 58201192 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (5-Chloro-4-methoxy-6-methylpyridin-3-yl)methanol | HCID 58201212 | 105.7% |
Reaction Steps
The above methyl 5-chloro-4-methoxy-6-methylnicotinate (1.0 g) was dissolved in 30 ml of methanol, and sodium borohydride (1.75 g) was then added to the solution. The resulting mixture was heated under reflux for 1 hour. Thereafter, a saturated ammonium chloride aqueous solution was added to the reaction solution under cooling on ice, followed by extraction with chloroform three times. The organic layer was dried over anhydrous sodium sulfate, and the solvent was then distilled away, so as to obtain the title compound (0.92 g) as an oily substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08815880B2 |
| Source dataset | uspto-grants-2014_08 |
| ORD ID | ord-8d23ab0fb31f4824a93a0bf305debbcb |
| Source note | uspto-grants-2014_08 |