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HRID 37441作成日:2026年10月24日

p-(2-(Dimethylamino)ethoxy)benzaldehyde → 2-[p-[(E)-2-(3,4-dihydro-4,4-dimethyl-2H--benzothiopyran-6-yl)propenyl]phenoxy]-N,N-dimethylethylamine

https://huagongshe.com/ja/reaction/37441

反応式

関与物質

役割名称HCID仕込み量
反応物p-(2-(Dimethylamino)ethoxy)benzaldehydeHCID 84823—
反応物[1-(4,4-Dimethyl-6-thiochromanyl)ethyl]triphenylphosphonium bromideHCID 19935432—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物2-[p-[(E)-2-(3,4-dihydro-4,4-dimethyl-2H--benzothiopyran-6-yl)propenyl]phenoxy]-N,N-dimethylethylamineHCID 6778346644.1%

反応条件

温度0 °C

反応手順

32 g of [1-(4,4-dimethyl-6-thiochromanyl)ethyl]triphenylphosphonium bromide were suspended in 130 ml of tetrahydrofuran and treated at 0° C. with 37 ml of n-butyllithium (1.6 molar in hexane). After stirring at 0° C. for 45 minutes, a solution of 10 g of 4-(2-dimethylaminoethoxy)benzaldehyde in 60 ml of tetrahydrofuran was added dropwise to the orange reaction mixture. The mixture was stirred at room temperature for an additional 1 hour, poured on to ice/water and extracted with ether. The organic phases were washed with water, dried and evaporated. After filtration of the crude product over neutral Alox (eluting agent ether) and recrystallization from hexane/ether, there were obtained 8.7 g of 2-[p-[(E)-2-(3,4-dihydro-4,4-dimethyl-2H-1-benzothiopyran-6-yl)propenyl]phenoxy]-N,N-dimethylethylamine, melting point 81°-82° 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-60610fa263774d419fa3d8889eeb31c1
出典メモuspto-grants-1995_05