HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl Peroxide → 3-Acetoxy-4-tert-butylbenzyl bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl Peroxide | HCID 7187 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 3-Acetoxy-4-tert-butyltoluene | HCID 21458781 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 3-Acetoxy-4-tert-butylbenzyl bromide | HCID 21458757 | — |
Reaction Steps
16.4 g of N-bromosuccinimide, 1 g of α,α'-azoisobutyronitrile and 1 g of dibenzoyl peroxide are added in succession to a solution, stirred at 70° C. of 19 g of 3-acetoxy-4-tert-butyltoluene in 900 ml of CCl4. The reaction mixture is stirred under reflux for 31/2 hours under UV irradiation and is filtered, and the filtrate is concentrated by evaporation. The title compound is obtained from the residue by means of FC (900 g of silica gel, hexane/ethyl acetate=95:5): Rf (hexane/ethyl acetate=95:5)=0.40.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05627182 |
| Source dataset | uspto-grants-1997_05 |
| ORD ID | ord-33603a99a2d644fd92a1d32ae243ef00 |
| Source note | uspto-grants-1997_05 |