Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 5,7-dibromoisatin | HCID 1809920 | — |
| Reactant | HCID 5324643 | HCID 5324643 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 178486607 | HCID 178486607 | — |
Reaction Steps
7.6 g (0.025 mol) of 5,7-dibromoisatin, 6.15 g (0.025 mol) of 5,7-di-tert-butyl-3H-benzofuran-2-one and 0.5 g of p-toluenesulfonic acid are boiled in 25 ml of acetic acid under nitrogen for 21 hours. 40 ml of methanol are then added and the suspension obtained is cooled to 5° C. The solid then obtained is filtered off and the filter residue is washed with methanol and dried at 60° C. The yield is 10.7 g (80% of theory). Melting point: 303-314° C. C: calculated/found 49.73/49.46; H: calculated/found 3.38/3.45; N: calculated/found 2.76/2.73
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06503937B1 |
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| Source dataset | uspto-grants-2003_01 |
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| ORD ID | ord-4231e7fd8dae404292584e5b9ed22bf0 |
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| Source note | uspto-grants-2003_01 |
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