HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → 4-(bromomethyl)-2-(2,4-difluorophenyl)-5-methyl-2H-1,2,3-triazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-(2,4-Difluorophenyl)-5-methyl-2H-1,2,3-triazole-4-methanol | HCID 90109252 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(bromomethyl)-2-(2,4-difluorophenyl)-5-methyl-2H-1,2,3-triazole | HCID 90111806 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
2-(2,4-Difluorophenyl)-5-methyl-2H-1,2,3-triazole-4-methanol (i.e. the product of Step B, 0.70 g, 3.1 mmol) was suspended in 48% hydrobromic acid in water (16 mL). The mixture was heated to reflux with stirring for 2 h. The reaction mixture was diluted with water, cooled to 0° C. and basified with 50% aqueous sodium hydroxide solution. The reaction mixture was extracted with ethyl acetate, dried (MgSO4) and concentrated under reduced pressure to obtain the title compound (0.75 g) as a pale yellow oil. The title compound was used directly in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09302999B2 |
| Source dataset | uspto-grants-2016_04 |
| ORD ID | ord-a51d8bcae5f847ad87bbdb9d4302abbb |
| Source note | uspto-grants-2016_04 |