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Chlorotrimethylsilane → Silane, 2,4-cyclopentadien-1-ylidenebis(trimethyl-
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Chlorotrimethylsilane | HCID 6397 | — |
| 反応物 | Sodium, 2,4-cyclopentadien-1-yl- | HCID 78681 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | Silane, 2,4-cyclopentadien-1-ylidenebis(trimethyl- | HCID 141813 | — |
| 生成物 | 1,3-Cyclopentadiene, (trimethylsilyl)- | HCID 12024673 | — |
反応手順
Trimethylsilylcyclopentadiene and bis(trimethylsilyl)cyclopentadiene are prepared by the procedures of Kraihanzel et al., J. Amer. Chem. Soc., 90, 4701 (1968) and I. M. Pribytkova et al., J. of Organometallic Chem., 30, C57-C60 (1971). Sodium cyclopentadienide (44 g, 0.50 mole) is added to 150 ml of tetrahydrofuran. Chlorotrimethylsilane (54 g, 0.5 mole) is added dropwise slowly to the reaction and the stirring is continued for 3 hours. The reaction mixture is poured into 150 ml of cold, distilled water and trimethylsilylcyclopentadiene is extracted into diethyl ether. The extract is rotary evaporated to remove the ethereal solvent and the residue is vacuum distilled to give trimethylsilylcyclopentadiene, b.p. 41° C.-43° C. (16 mm).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04717783 |
| 出典データセット | uspto-grants-1988_01 |
| ORD ID | ord-218c7105e6b84503bb205e22ddcde047 |
| 出典メモ | uspto-grants-1988_01 |