HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → Ethyl 1-methyl-1-(4-bromomethylphenyl)ethanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Ethyl 1-methyl-1-(4-methylphenyl)ethanesulfonate | HCID 21706484 | — |
| Catalyst | Benzoyl chloride | HCID 7412 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | Ethyl 1-methyl-1-(4-bromomethylphenyl)ethanesulfonate | HCID 21706518 | 105.4% |
Reaction Steps
To a solution of ethyl 1-methyl-1-(4-methylphenyl)ethanesulfonate (0.458 g, 1.89 mmol) in carbon tetrachloride (8 mL) was added N-bromosuccinimide (0.370 g, 2.08 mmol) and benzoyl chloride (0.009 g). The mixture was heated under reflux for 1.5 hours, cooled to rt, and filtered. The filtrate was washed with aqueous sodium bicarbonate and brine, dried, filtered and evaporated to give crude ethyl 1-methyl-1-(4-bromomethylphenyl)ethanesulfonate (0.64 g, 100%) which was used directly in the next reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06156784 |
| Source dataset | uspto-grants-2000_12 |
| ORD ID | ord-cf19bccbd6f64581b27e7e93d4e3d6df |
| Source note | uspto-grants-2000_12 |