化工社化工社 化学情報印刷レポート · 研究参考用
Dichlorodimethylsilane → Chloro(4,5-dimethyl-6H-cyclopenta[b]thien-6-yl)dimethylsilane
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Dichlorodimethylsilane | HCID 6398 | — |
| 反応物 | 4,5-dimethyl-4H-cyclopenta[b]thiophene | HCID 12307588 | — |
| 反応物 | 4,5-dimethyl-6H-cyclopenta[b]thiophene | HCID 66809306 | — |
| 反応物 | Butyllithium | HCID 178418339 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | Chloro(4,5-dimethyl-6H-cyclopenta[b]thien-6-yl)dimethylsilane | HCID 58526148 | — |
反応手順
Under an argon atmosphere, to a solution of 10.0 g (66.6 mmol) of a mixture of 4,5-dimethyl-4H-cyclopenta[b]thiophene and 4,5-dimethyl-6H-cyclopenta[b]thiophene in 150 ml of THF, 26.6 ml of 2.5 M (66.6 mmol) nBuLi in hexanes was added dropwise over 30 minutes at −60° C. This mixture was additionally stirred for 2 hours at room temperature and then added dropwise for 3 hours to a solution of 23.7 ml (25.2 g, 200 mmol) of dichlorodimethylsilane in 50 ml of THF. The resulting mixture was stirred for 12 hours at ambient temperature and then evaporated to dryness. Fractional distillation gave yellowish liquid, by 83-85° C./0.2 mm Hg. Yield 10.7 g (66%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08173828B2 |
| 出典データセット | uspto-grants-2012_05 |
| ORD ID | ord-c86c913e4cf0472ca99fb4acc2c8e311 |
| 出典メモ | uspto-grants-2012_05 |