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HRID 977913作成日:2026年10月25日

Tetrahydrofuran → Silane, (chloromethyl)(4-ethoxyphenyl)dimethyl-

https://huagongshe.com/reaction/977913

反応式

関与物質

役割名称HCID仕込み量
反応物TetrahydrofuranHCID 8028—
反応物4-BromophenetoleHCID 68523—
反応物Silane, chloro(chloromethyl)dimethyl-HCID 74393—
反応物ButyllithiumHCID 178418339—
溶媒WaterHCID 962—
溶媒Ethyl AcetateHCID 8857—
生成物Silane, (chloromethyl)(4-ethoxyphenyl)dimethyl-HCID 18471749.8%

反応条件

温度-78 °C

反応手順

A mixture of 60 ml of THF, p-bromophenetole (9.7 gram) and chloromethyldimethylsilyl chloride (7.3 gram) was cooled in a dry ice/acetone bath. To the mixture was dropwise added 33 ml of 1.55M n-butyl lithium under an argon atmosphere. After stirring the mixture for additional 15 minutes at -78° C., the stirring was continued at room temperature for 30 minutes. The mixture was added with 6 ml of ethyl acetate and 30 ml of water, and extracted with ethyl ether. The ether extract was washed with saturated sodium chloride solution, dried, and concentrated. Distillation of the residue gave 5.5 gram of chloromethyldimethyl(4-ethoxyphenyl)silane. Physicochemical data of the product is listed in Table 3.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04663314
出典データセットuspto-grants-1987_05
ORD IDord-b1065096d3b94e748a4c45e61f4fe559
出典メモuspto-grants-1987_05