HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl Peroxide → HCID 14153223, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl Peroxide | HCID 7187 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Methyl 3-[(dimethylamino)sulfonyl]-2-methylbenzoate | HCID 13937642 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | HCID 14153223 | HCID 14153223 | — |
Reaction Steps
A mixture of 25.7 g of the product from Example 10, 17.8 g of N-bromosuccinimide, and 1.0 g benzoyl peroxide in 350 ml carbon tetrachloride was stirred at reflux temperature for 3.5 hours and then at room temperature overnight. The by-product succinimide was removed by filtration and the filtrate concentrated in vacuo to afford an oil which was dissolved in ether and washed with two portions of water. Drying and evaporation of the ether layer afforded a viscous yellow oil which was shown by 1H NMR analysis to consist of the title compound and unreacted starting material in a ratio of approximately 2:1. This mixture was carried directly on to the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04737185 |
| Source dataset | uspto-grants-1988_04 |
| ORD ID | ord-5baf883a48694dc7a2b98e617f92323f |
| Source note | uspto-grants-1988_04 |