HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl Peroxide → 2-(2-Bromomethylphenyl)-2-difluoromethoxyimino-acetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl Peroxide | HCID 7187 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | alpha-Difluoromethoxyimino-o-tolylacetonitrile | HCID 57050284 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 2-(2-Bromomethylphenyl)-2-difluoromethoxyimino-acetonitrile | HCID 54541296 | — |
Reaction Steps
A solution of 8.0 g of α-difluoromethoxyimino-o-tolylacetonitrile and 0.07 g of dibenzoyl peroxide in 50 ml of carbon tetrachloride is heated to reflux. With radiation from a lamp, 6.77 g of N-bromosuccinimide are added thereto in several small portions and the mixture is left to react for 0.5 hour. The reaction mixture is cooled to room temperature, the succinimide is filtered off and the residue is concentrated by evaporation. Chromatography on silica gel with hexane/ethyl acetate (15:1) yields pure 2-(2-bromomethylphenyl)-2-difluoromethoxyimino-acetonitrile in the form of a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05710314 |
| Source dataset | uspto-grants-1998_01 |
| ORD ID | ord-88301543e6554e70a4fe4e70b4bf86b8 |
| Source note | uspto-grants-1998_01 |