関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 2,7-Dibromo-9-(bis-methylsulfanyl-methylene)fluorene | HCID 12151612 | — |
| 反応物 | HCID 178443577 | HCID 178443577 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 2,7-Dibromo-9-(bisoctyl-methylene)fluorene | HCID 12151616 | — |
反応手順
To a solution of 2,7-dibromo-9-(bis-methylsulfanyl-methylene)fluorene (5.1 g, 12 mmol) in dry THF (100 ml) at 0° C. under nitrogen, was added a solution of lithium tetrachlorocuprate (5 ml of a 0.1 M solution in THF, 5 mol %). A solution of octylmagnesium bromide (13 ml of a 2.0M solution in diethyl ether, 0.026 mol) was added dropwise over 30 min. The reaction was stirred for 2 h at 5° C. The reaction was cooled to 0° C. and further lithium tetrachlorocuprate (1 ml of a 0.1M solution in THF, 1 mol %) was added. The reaction was then stirred for 24 h at 15° C., before quenching and workup as above. Yield (60%). Purity (HPLC>99%). 1H and 13C NMR spectra as expected. M+=560 (t).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06943275B2 |
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| 出典データセット | uspto-grants-2005_09 |
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| ORD ID | ord-a5ba07bf6a4d4964add042633a80500c |
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| 出典メモ | uspto-grants-2005_09 |
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