참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1,2-Dibromobenzene | HCID 11414 | — |
| 반응물 | 9-Anthraceneboronic Acid | HCID 15510213 | — |
| 생성물 | 1,2-Bis(anthracen-9-yl)benzene | HCID 57702512 | — |
반응 단계
Procedure analogous to Example 3a. Instead of 149.0 ml (1.2 mol) of 1,2-dibromobenzene and 98.0 g (308 mmol) of 9,10-anthracenediboronic acid ethylene glycol ester, 12.1 ml (100 mmol) of dibromobenzene and 68.0 g (306 mmol) of 9-anthraceneboronic acid are used. After cooling, the solid is filtered off with suction, washed three times with 100 ml of ethanol each time and then washed twice by stirring with 1000 ml of refluxing acetic acid each time (1 h) and each time filtered off with suction after cooling to 90° C. The mother liquor is discarded in each case. The solid is finally washed once with boiling ethanol. Yield: 33.0 g (76 mmol), 76.6% of theory; purity: 98% according to 1H-NMR.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08674141B2 |
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| 출처 데이터셋 | uspto-grants-2014_03 |
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| ORD ID | ord-6e6b71dab2514ea1be14abefbfe8b265 |
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| 출처 메모 | uspto-grants-2014_03 |
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