関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Methanol | HCID 887 | — |
| 反応物 | Furan | HCID 8029 | — |
| 反応物 | Benzene, 1,2,4,5-tetrabromo-3,6-dimethyl- | HCID 31952 | — |
| 反応物 | Butyllithium | HCID 178418339 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | 5,6-Dibromo-4,7-dimethyl-1,4-epoxy-1,4-dihydronaphthalene | HCID 22678912 | 50% |
反応手順
To tetrabromo para-xylene (2.1 g, 5.0 mmol) and furan (4 g, 58.8 mmol) in PhMe (55 mL) at −78° C. was added BuLi (2.2 mL, 2.5M in hexanes, 5.5 mmol) dropwise. The reaction was stirred for two hours at −78° C. and the allowed to warm to rt. After 3 hours, MeOH (2 mL) was added and the reaction mixture was poured into water. The organic layer was separated and the aqueous layer was extracted three times with Et2O. The combined organic layers were washed with brine, dried over MgSO4, and concentrated. Flash chromatography on silca gel gave 26 (185 mg, 50%) as a white solid. The spectral data correlates well with the literature values. 22
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07420003B2 |
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| 出典データセット | uspto-grants-2008_09 |
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| ORD ID | ord-d83172b32ece455e8c15e3a664faf33b |
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| 出典メモ | uspto-grants-2008_09 |
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