戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1980502作成日:2026年10月27日

p-Bromochlorobenzene → (Chloromethyl)(4-chlorophenyl)dimethylsilane

https://huagongshe.com/reaction/1980502

反応式

関与物質

役割名称HCID仕込み量
反応物p-BromochlorobenzeneHCID 7806—
反応物Silane, chloro(chloromethyl)dimethyl-HCID 74393—
反応物ButyllithiumHCID 178418339—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
溶媒HexaneHCID 8058—
溶媒Lithium ChlorideHCID 433294—
生成物(Chloromethyl)(4-chlorophenyl)dimethylsilaneHCID 273308955%

反応手順

A solution of 9.6 g (0.050 mol) of 4-bromochlorobenzene and 6.6 ml (7.2 g, 0.050 mol) of chlorochloromethyldimethylsilane in 75 ml of tetrahydrofuran was stirred at -78° under nitrogen while 31 ml (0.050 mol) of 1.6 molar n-butyllithium in hexane was added dropwise. The resulting clear solution was allowed to warm to room temperature, diluted with ether until no more lithium chloride precipitated, and filtered. Evaporation of the filtrate left 10.6 g of a light yellow liquid, which was distilled to give 6.0 g (55%) of the title compound as a colorless liquid: bp 54°-58° C. (0.05 mm); ir (neat) 2910, 1560, 1470, 1370, 1250, 1080, 1010, 840, 805, 790, 740 cm-1 ; nmr (CDCl3) 0.4 (6H, s), 2.9 (2H, s), 7.1-7.6 (4H, q).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04510136
出典データセットuspto-grants-1985_04
ORD IDord-31f44f32b71a4cc8a21c2ae6682da9d5
出典メモuspto-grants-1985_04