関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Veratraldehyde | HCID 8419 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | Diethyl (1,3-Dithian-2-yl)phosphonate | HCID 10869064 | — |
| 触媒 | Benzyl triethylammonium chloride | HCID 66133 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 2-[(3,4-Dimethoxyphenyl)methylidene]-1,3-dithiolane | HCID 23039000 | — |
反応手順
A solution of 2-diethoxyphosphoryl-1,3-dithiane (23.4 g) and 3,4-dimethoxybenzaldehyde (16.0 g) in dichloromethane (70 ml) is added to a mixture of dichloromethane (85 ml), a 50% aqueous solution of sodium hydroxide (170 ml) and triethylbenzylammonium chloride (1.4 g). The mixture is stirred for 24 hours at room temperature. The two phases are then separated. The aqueous solution is extracted with dichloromethane (100 ml) and the combined organic solutions are washed with a 10% aqueous solution of ammonium chloride (3×100 ml) and with water (2×100 ml). The dichloromethane is dried over magnesium sulphate and evaporated in vacuo. The residue is purified by column chromatography on silica gel using chloroform as eluant. The product is dried in vacuo to constant weight to yield (1,3-dithiolan-2-ylidene)-(3,4-dimethoxyphenyl)-methane, m.p. 74°-75°.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04818765 |
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| 出典データセット | uspto-grants-1989_04 |
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| ORD ID | ord-0f37c9248a30456a9319dc2d4ac67112 |
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| 出典メモ | uspto-grants-1989_04 |
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