Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzoyl Peroxide | HCID 7187 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 66893378 | HCID 66893378 | — |
| Solvent | Chlorobenzene | HCID 7964 | — |
| Product | HCID 66893431 | HCID 66893431 | — |
Reaction Steps
Methyl 5-[(2-methoxy-5-methylphenyl)sulfonyl]-2,3-dihydro-1-benzofuran-7-carboxylate (879 mg, 2.4 mmol; Intermediate 66) was dissolved in chlorobenzene (6 mL). N-bromosuccinimide (432 mg, 2.4 mmol) and benzoyl peroxide (58 mg, 0.24 mmol) were added and the mixture was stirred at 100° C. for 17 h. The mixture was washed with saturated aqueous NaHCO3 and the organic layer was concentrated. Yield: 405 mg (46%) after purification by preparative HPLC (System F; 40-60% MeCN). MS (ESI+) for C18H16O6S m/z 361 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07820675B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-50b7b58b2472489db228e6f8ed27932b |
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| Source note | uspto-grants-2010_10 |
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