참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Methanol | HCID 887 | — |
| 반응물 | Furan | HCID 8029 | — |
| 반응물 | Benzene, 1,2,4,5-tetrabromo-3,6-dimethyl- | HCID 31952 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | 5,6-Dibromo-4,7-dimethyl-1,4-epoxy-1,4-dihydronaphthalene | HCID 22678912 | 50% |
반응 단계
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
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07420003B2 |
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| 출처 데이터셋 | uspto-grants-2008_09 |
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| ORD ID | ord-d83172b32ece455e8c15e3a664faf33b |
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| 출처 메모 | uspto-grants-2008_09 |
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