HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl Peroxide → Bromo-(4-chlorosulfonyl-phenyl)-acetic acid ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl Peroxide | HCID 7187 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | (4-Chlorosulfonyl-phenyl)-acetic acid ethyl ester | HCID 10467900 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | Bromo-(4-chlorosulfonyl-phenyl)-acetic acid ethyl ester | HCID 59610030 | 94.4% |
Reaction Steps
(4-Chlorosulfonyl-phenyl)-acetic acid ethyl ester (1.6 gm, 6.45 mmol) was taken in carbon tetrachloride (13 ml). N-Bromosuccinimide (1.26 gm, 7.09 mmol) was added in one lot followed by benzoyl peroxide (171 mg, 0.7 mmol). The reaction mixture was refluxed for 2 days. The reaction mixture was cooled to room temperature and filtered; filtrate was washed with water followed by brine solution, dried over anhydrous sodium sulfate and concentrated under reduced pressure to provide bromo-(4-chlorosulfonyl-phenyl)-acetic acid ethyl ester (2.08 gm) as a gummy mass. The crude material was used as such for further reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08501955B2 |
| Source dataset | uspto-grants-2013_08 |
| ORD ID | ord-bbfbe1f19fe142cb8955f006d7e9de3d |
| Source note | uspto-grants-2013_08 |