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HRID 726828作成日:2026年10月27日

Iodine → [(S)-2-methylbutyl]phenyldichlorosilane

https://huagongshe.com/reaction/726828

反応式

関与物質

役割名称HCID仕込み量
反応物IodineHCID 807—
反応物PhenyltrichlorosilaneHCID 7372—
反応物MagnesiumHCID 5462224—
反応物1-Bromo-2-methylbutane, (+)-HCID 5464167—
溶媒TetrahydrofuranHCID 8028—
溶媒HexaneHCID 8058—
生成物[(S)-2-methylbutyl]phenyldichlorosilaneHCID 67606162—

反応手順

Anhydrous tetrahydrofuran (125 mL) was put into a reactor with magnesium (5.7 g, 0.24 mol) and molecular sieves 4A which had been dehydrated and deaerated, followed by charging of argon gas. A small amount of iodine was slowly added to the mixture. (S)-(+)-1-bromo-2-methylbutane (30 g, 0.20 mol) was added dropwise to the slowly stirred mixture so that the reaction mixture was gradually refluxed. After the reaction was complete, the obtained Grignard reagent was transferred to a dropping funnel. The Grignard reagent was added dropwise to a solution being stirred containing phenyltrichlorosilane (50 g, 0.24 mol) in anhydrous tetrahydrofuran (50 mL) in another reactor which had been dehydrated and deaerated, followed by charging of argon gas, at 40° C.-50° C. The reaction mixture was then stirred overnight at room temperature. Hexane (500 mL) was added to the reaction mixture, and the resulting mixture was filtered under pressure, followed by fractional distillation of the filtrate to provide the desired product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05710301
出典データセットuspto-grants-1998_01
ORD IDord-68b0b1270932435b9b009a92f1bad50d
出典メモuspto-grants-1998_01