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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
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | p-(2-(Dimethylamino)ethoxy)benzaldehyde | HCID 84823 | — |
| 反応物 | [1-(4,4-Dimethyl-6-thiochromanyl)ethyl]triphenylphosphonium bromide | HCID 19935432 | — |
| 反応物 | Butyllithium | HCID 178418339 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 2-[p-[(E)-2-(3,4-dihydro-4,4-dimethyl-2H--benzothiopyran-6-yl)propenyl]phenoxy]-N,N-dimethylethylamine | HCID 67783466 | 44.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05420273 |
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| 出典データセット | uspto-grants-1995_05 |
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| ORD ID | ord-60610fa263774d419fa3d8889eeb31c1 |
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| 出典メモ | uspto-grants-1995_05 |
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