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HRID 248567作成日:2026年10月26日

Sulfuric Acid → 1-Chloro-4-(1-trimethylsilylhexyl)benzene

https://huagongshe.com/reaction/248567

反応式

関与物質

役割名称HCID仕込み量
反応物Sulfuric AcidHCID 1118—
反応物ChlorotrimethylsilaneHCID 6397—
反応物1-(6-Bromohexyl)-4-chlorobenzeneHCID 580679—
反応物MagnesiumHCID 5462224—
触媒Copper;dilithium;tetrachlorideHCID 193501—
触媒1-(6-Bromohexyl)-4-chlorobenzeneHCID 580679—
溶媒TetrahydrofuranHCID 8028—
溶媒tert-Butyl methyl etherHCID 15413—
生成物1-Chloro-4-(1-trimethylsilylhexyl)benzeneHCID 1976385939%

反応条件

温度60 °C

反応手順

Approximately 2 g (82 mMol) of magnesium in a flask were moistened with tetrahydrofuran. A Grignard reaction was initiated using 5 drops of 1-(6-bromohexyl)-4-chlorobenzene. The remainder of a total of 17 g of the halogen compound (61 mMol), dissolved in 50 ml of tetrahydrofuran, was added dropwise at 50° to 60° C. When the addition was complete, the mixture was kept at this temperature for an additional 2.5 hours, and a solution of 12 g (110 mMol) of trimethylchlorosilane and a catalytic amount of dilithium tetrachlorocuprate in 40 ml of tetrahydrofuran was then added dropwise at 20° to 40° C. The mixture was stirred at 60° C. for 1 hour, then allowed to stand overnight and diluted with 200 ml of tert-butyl methyl ether. The mixture was then acidified using 2N sulfuric acid, the phases were separated, and the organic phase was washed and dried. The evaporated residue was fractionated. About 6.4 g of 1-chloro-4-(1-trimethylsilylhexyl)benzene (38.6 percent yield) were obtained at a pressure of 0.2 hPa and at 88° to 90° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05210247
出典データセットuspto-grants-1993_05
ORD IDord-199d6f6eb60e456080d3e5aa1cc42175
出典メモuspto-grants-1993_05