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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1072783생성일: 2026년 10월 27일

Chlorotrimethylsilane → 1-(2,4-Dichlorophenyl)-1-trimethylsilyloxyethene

https://huagongshe.com/reaction/1072783

반응식

참여 물질

역할이름HCID투입량
반응물ChlorotrimethylsilaneHCID 6397—
반응물DiisopropylamineHCID 7912—
반응물2',4'-DichloroacetophenoneHCID 16693—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
용매HexamethylphosphoramideHCID 12679—
생성물1-(2,4-Dichlorophenyl)-1-trimethylsilyloxyetheneHCID 22388270—

반응 단계

Diisopropylamine (16.2 g) was dissolved in tetrahydrofuran (133 ml), and 1.6N n-butyl lithium (100 ml) was dropwise added thereto under ice-cooling. The reaction mixture was stirred at the same temperature for 10 min, and a solution of 2,4-dichloroacetophenone (25.2 g) in tetrahydrofuran (133 ml) was dropwise added under cooling in a dry ice-acetone bath. Hexamethylphosphoramide (26.7 ml) was added little by little. The mixture was stirred at the same temperature for 5 min, and chlorotrimethylsilane (20.3 ml) was dropwise added, which was followed by stirring at room temperature for 30 min. The reaction mixture was partitioned between ice-cooled n-hexane and ice-cooled water. The organic layer was washed twice with ice-cooling water and then once with saturated brine, dried over sodium sulfate and concentrated under reduced pressure to dryness to give a crude product (37.5 g) of the objective compound as a pale-yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06911469B2
출처 데이터셋uspto-grants-2005_06
ORD IDord-f1de138c6b3e4ae9998fdfbbd3b09491
출처 메모uspto-grants-2005_06