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HRID 2413505作成日:2026年10月25日

Chlorotrimethylsilane → Silane, 2,4-cyclopentadien-1-ylidenebis(trimethyl-

https://huagongshe.com/reaction/2413505

反応式

関与物質

役割名称HCID仕込み量
反応物ChlorotrimethylsilaneHCID 6397—
反応物Sodium, 2,4-cyclopentadien-1-yl-HCID 78681—
溶媒TetrahydrofuranHCID 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

DOI10.6084/m9.figshare.5104873.v1
特許番号US04717783
出典データセットuspto-grants-1988_01
ORD IDord-218c7105e6b84503bb205e22ddcde047
出典メモuspto-grants-1988_01