HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Chloride → (1-(4-Fluorophenyl)-4-methyl-1H-1,2,3-triazol-5-yl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 1-(4-Fluorophenyl)-4-methyl-1H-1,2,3-triazole-5-carbaldehyde | HCID 19914653 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (1-(4-Fluorophenyl)-4-methyl-1H-1,2,3-triazol-5-yl)methanol | HCID 19914681 | 89.9% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
To a solution of 3-(4-fluoro-phenyl)-5-methyl-3H-[1,2,3]triazole-4-carbaldehyde (2.28 g, 11 mmol) in MeOH (180 mL) was added sodiumborohydride (210 mg, 6.0 mmol) at 0° C., and the resulting mixture stirred at 0° C. for 30 min, The mixture was then poured into saturated ammonium chloride solution and extracted with ethyl acetate and the combined organic extracts washed with brine, dried over sodium sulphate, filtered and evaporated to afford the title compound (2.05 g, 89%) as a white solid. MS: m/e=208.2 [M]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08742097B2 |
| Source dataset | uspto-grants-2014_06 |
| ORD ID | ord-1e0d29d99b474aa2a2ddb130434e0034 |
| Source note | uspto-grants-2014_06 |