HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Chloride → (3,5-Difluoropyridin-2-YL)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Ethyl 3,5-difluoropyridine-2-carboxylate | HCID 46311358 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (3,5-Difluoropyridin-2-YL)methanol | HCID 53414314 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
To a solution of 3,5-difluoro-pyridine-2-carboxylic acid ethyl ester of part A (2.5 g, 12.6 mmol) in ethanol (10 mL), cooled using an ice water bath, was added sodium borohydride (1.43 g, 37.8 mmol) in a portion wise manner. The solution was stirred at 0° C. for thirty minutes and at ambient temperature for 2 h. The reaction was returned to 0° C. and saturated ammonium chloride was added dropwise. The solvent was removed in vacuo and the resulting residue was partitioned between ethyl acetate and water. The organic layer was washed with saturated ammonium chloride, water and brine, and dried over magnesium sulfate. The slurry was filtered and concentrated to provide the alcohol as a yellow oil (1.8 g): MS (ES) m/e 146 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09115089B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-777de6ad333744ed95c335ee23cc25e4 |
| Source note | uspto-grants-2015_08 |