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HRID 1922321作成日:2026年10月24日

Dichlorodimethylsilane → Chloro(4,5-dimethyl-6H-cyclopenta[b]thien-6-yl)dimethylsilane

https://huagongshe.com/ja/reaction/1922321

反応式

関与物質

役割名称HCID仕込み量
反応物DichlorodimethylsilaneHCID 6398—
反応物4,5-dimethyl-4H-cyclopenta[b]thiopheneHCID 12307588—
反応物4,5-dimethyl-6H-cyclopenta[b]thiopheneHCID 66809306—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物Chloro(4,5-dimethyl-6H-cyclopenta[b]thien-6-yl)dimethylsilaneHCID 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

DOI10.6084/m9.figshare.5104873.v1
特許番号US08173828B2
出典データセットuspto-grants-2012_05
ORD IDord-c86c913e4cf0472ca99fb4acc2c8e311
出典メモuspto-grants-2012_05