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HRID 247457作成日:2026年10月26日

Allyl bromide → Methyl alpha-ethyl-alpha-2-propenylbenzeneacetate

https://huagongshe.com/reaction/247457

反応式

関与物質

役割名称HCID仕込み量
反応物Allyl bromideHCID 7841—
反応物DiisopropylamineHCID 7912—
反応物Benzeneacetic acid, alpha-ethyl-, methyl esterHCID 102780—
反応物ButyllithiumHCID 178418339—
溶媒MethanolHCID 887—
溶媒TetrahydrofuranHCID 8028—
溶媒HexaneHCID 8058—
生成物Methyl alpha-ethyl-alpha-2-propenylbenzeneacetateHCID 13678420—

反応手順

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:

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04707499
出典データセットuspto-grants-1987_11
ORD IDord-3dceaf1bd6054f02adc274c997239858
出典メモuspto-grants-1987_11