Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 1,2-dimethoxynaphthalene | HCID 299257 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22452676 | HCID 22452676 | 68.6% |
Reaction Steps
To the solution of 1,2-dimethoxynaphthalene (3.83 g, 20.3 mmol) in THF (100 mL) was added dropwise at 0° C. a solution of NBS (3.62 g, 20.3 mmol) in THF (50 mL). After stirring at 0° C. for 0.5 h, the solvent was removed in vacuo and CCl4 was added. The mixture was filtered and the filtrate was concentrated. Column chromatography yielded the title compound as a yellow oil (3.72 g, 68%). 1H NMR (CDCl3) δ 8.1 (m, 2H), 7.60 (s, 1H), 7.49 (m, 2H), 3.99 (s, 3H) 3.98 (s, 3H); MS m/z 267 (M−H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06403601B1 |
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| Source dataset | uspto-grants-2002_06 |
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| ORD ID | ord-b699603df0fd4f78850183351de30738 |
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| Source note | uspto-grants-2002_06 |
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