Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 6-difluoromethoxy-3H-isobenzofuran-1-one | HCID 18381606 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 18381642 | HCID 18381642 | 101.1% |
Reaction Steps
A suspension of 6-difluoromethoxy-3H-isobenzofuran-1-one (1 g, 5 mmoles), prepared as described in example 94, in CCl4 (10 ml), under N2, was added with N-bromosuccinimide (0.91 g, 5.1 mmoles) and the mixture was heated at 76° C. A solution of α,α′-azaisobutyronitrile (0.01 g) in CHCl3 (1 ml) was slowly added. The mixture was refluxed for 1.5 hours, then cooled, filtered over celite and washed with CCl4. By drying, 1.41 g of the title compound were obtained as an oil (quantitative yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06329370B1 |
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| Source dataset | uspto-grants-2001_12 |
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| ORD ID | ord-66632c421aec40a4a3b4c9e3c8f9979e |
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| Source note | uspto-grants-2001_12 |
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