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HRID 37430作成日:2026年10月24日

4-(2-Morpholinoethoxy)benzaldehyde → 4-[2-[p-[(E)-2-(2,2-dimethyl-1,3-benzodithiol-5-yl)propenyl]phenoxy]ethyl]morpholine

https://huagongshe.com/ja/reaction/37430

反応式

関与物質

役割名称HCID仕込み量
反応物4-(2-Morpholinoethoxy)benzaldehydeHCID 3719902—
反応物[1-(2,2-Dimethyl-1,3-benzodithiol-5-yl)ethyl]triphenylphosphonium bromideHCID 19935456—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
溶媒HexaneHCID 8058—
生成物4-[2-[p-[(E)-2-(2,2-dimethyl-1,3-benzodithiol-5-yl)propenyl]phenoxy]ethyl]morpholineHCID 8674496235.2%

反応条件

温度20 °C

反応手順

6.6 g of [1-(2,2-dimethyl-1,3-benzodithiol-5-yl)ethyl]triphenylphosphonium bromide were dissolved in 40 ml of tetrahydrofuran and treated slowly at 0° C. with 9 ml of a 1.5 molar solution of n-butyllithium in hexane. After 40 minutes, 3.5 g of 4-(2-morpholinoethoxy)benzaldehyde in 10 ml of tetrahydrofuran were added dropwise to the dark red solution and the mixture was stirred at 20° C. for 16 hours. The mixture was then poured on to ice and extracted with ethyl acetate. The combined extracts were washed with water, dried and evaporated. After chromatography (silica gel, eluting agent ethyl acetate) and crystallization from ether/hexane, there were obtained 1.8 g of 4-[2-[p-[(E)-2-(2,2-dimethyl-1,3-benzodithiol-5-yl)propenyl]phenoxy]ethyl]morpholine in the form of colorless crystals, melting point 90°-91° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05420273
出典データセットuspto-grants-1995_05
ORD IDord-42837d0913d74dd8bbe8aa52a66453a6
出典メモuspto-grants-1995_05