참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1,2-Dibromoethane | HCID 7839 | — |
| 반응물 | 4,7-dimethyl-1H-indene | HCID 81458 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 반응물 | HCID 178506817 | HCID 178506817 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 1H-Indene, 3,3'-(1,2-ethanediyl)bis[4,7-dimethyl- | HCID 10859990 | 48% |
반응 단계
38.2 g (265 mmol) of 4,7-dimethylindene was dissolved in 350 ml of tetrahydrofuran and the solution was cooled to 0° C. Then 165 ml of n-butyllithium (1,6M in hexane, 264 mmol) was added dropwise over 2.5 hours. After warming to room temperature and stirring for 4 hours a purple solution of 4,7-dimethylindenyl-lithium was obtained. This solution was cooled to -70° C. and treated dropwise with 25,3 g of 1,2-dibromoethane (135 mmol) in 15 ml of tetrahydrofuran over 35 min. After warming to room temperature, a pale yellow solution was obtained, and then water was added. The organic phase was collected and dried over Na2SO4. The solvent was removed by vacuum evaporation to provide 20 g of crude product (48% yield).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US05565533 |
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| 출처 데이터셋 | uspto-grants-1996_10 |
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| ORD ID | ord-d661a9859bd947ce97004226853d618c |
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| 출처 메모 | uspto-grants-1996_10 |
|---|