HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → Methyl 4-(bromomethyl)-3-(trifluoromethyl)benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Benzyl Peroxide | HCID 11229634 | — |
| Reactant | Methyl 4-methyl-3-(trifluoromethyl)benzoate | HCID 11952921 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | Methyl 4-(bromomethyl)-3-(trifluoromethyl)benzoate | HCID 57443327 | 88% |
Reaction Steps
A reactor is charged with 1 g (4.6 mmol) of the compound obtained in step 1, 0.97 g (5.5 mmol) of N-bromosuccinimide, 133 mg (0.55 mmol) of benzyl peroxide and 25 ml of carbon tetrachloride. The mixture is heated for 4 hours at reflux. The solvent is evaporated under reduced pressure and 100 ml of a saturated sodium bicarbonate solution is added. The solution obtained is extracted with 3*30 ml ethyl acetate. The organic phases are combined, dried on sodium sulphate and evaporated under reduced pressure to give the expected product (1.2 g, 88%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08580815B2 |
| Source dataset | uspto-grants-2013_11 |
| ORD ID | ord-5bf4e393be844e13b19d167f2911719e |
| Source note | uspto-grants-2013_11 |