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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 247457생성일: 2026년 10월 25일

Allyl bromide → HCID 13678420, 화합물

https://huagongshe.com/reaction/247457

반응식

참여 물질

역할이름HCID투입량
반응물Allyl bromideHCID 7841—
반응물DiisopropylamineHCID 7912—
반응물Benzeneacetic acid, alpha-ethyl-, methyl esterHCID 102780—
반응물ButyllithiumHCID 178418339—
용매MethanolHCID 887—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물HCID 13678420HCID 13678420—

반응 단계

To 15.4 ml of diisopropylamine in 400 ml of dry tetrahydrofuran at -20° to -30° under nitrogen atmosphere was added dropwise with stirring 64.3 ml of a 1.71 M solution of butyllithium in hexane. After stirring 15 min., the mixture was cooled to -70° and a solution of 17.8 g of methyl 2-phenylbutyrate in 100 ml of tetrahydrofuran was added dropwise. After stirring 30 min., a solution of 19.9 ml of allyl bromide in 50 ml tetrahydrofuran was added dropwise; the mixture was stirred and allowed to warm to room temperature overnight. After decomposing with methanol, the reaction mixture was concentrated in vacuo and the residue dissolved in diethyl ether. The ether solution was washed successively with dilute hydrochloric acid, water, dilute sodium bicarbonate, and saturated sodium chloride solution, then dried over anhydrous potassium carbonate and concentrated in vacuo. Distillation of the residue yielded 20.2 g of the title compound as a water-white oil, b.p. 84°-86°/0.45 mm, having the following elemental analysis:

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04707499
출처 데이터셋uspto-grants-1987_11
ORD IDord-3dceaf1bd6054f02adc274c997239858
출처 메모uspto-grants-1987_11