참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Tetrahydrofuran | HCID 8028 | — |
| 반응물 | 4-Octyne | HCID 16029 | — |
| 반응물 | 2,3-Bis(2-hexynyl)-1,4-dipropylnaphthalene | HCID 11394677 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 생성물 | 1,2,3,4,6,11-Hexapropyl-5,12-dihydrotetracene | HCID 17839509 | 46% |
반응 단계
2,3-Bis(2-hexynyl)-1,4-dipropylnaphthalene (0.373 g, 1.0 mmol) was added at −78° C. to a 20 ml THF solution of bis(i5-cyclopentadienyl)dibutylzirconium, which was prepared from bis(η5-cyclopentadienyl)dichlorozirconium (0.351 g, 1.2 mmol) and n-butyl lithium (1.5 ml, 2.4 mmols, 1.6 M). After elevating to room temperature, the reaction mixture was stirred for an hour. 4-Octyne (0.22 ml, 1.5 mmol) and NiBr2(PPh3)2 (0.892 g, 1.2 mmol) were added to the reaction mixture at room temperature. After stirring for 24 hours, hydrolysis was effected by 3N HCl followed by extraction with hexane. The extract was washed with sodium hydrogencarbonate aqueous solution and brine followed by drying over anhydrous magnesium sulfate. Column chromatography was performed using silica gel as the packing material to give the title compound (0.224 g) as somewhat orange powders by floured with ethanol. The isolation yield was 46%.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07901594B2 |
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| 출처 데이터셋 | uspto-grants-2011_03 |
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| ORD ID | ord-aab044d75960450bbc543654efb1a860 |
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| 출처 메모 | uspto-grants-2011_03 |
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