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HRID 620065作成日:2026年10月27日

Veratraldehyde → 2-[(3,4-Dimethoxyphenyl)methylidene]-1,3-dithiolane

https://huagongshe.com/reaction/620065

反応式

関与物質

役割名称HCID仕込み量
反応物VeratraldehydeHCID 8419—
反応物Sodium HydroxideHCID 14798—
反応物Diethyl (1,3-Dithian-2-yl)phosphonateHCID 10869064—
触媒Benzyl triethylammonium chlorideHCID 66133—
溶媒DichloromethaneHCID 6344—
生成物2-[(3,4-Dimethoxyphenyl)methylidene]-1,3-dithiolaneHCID 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

DOI10.6084/m9.figshare.5104873.v1
特許番号US04818765
出典データセットuspto-grants-1989_04
ORD IDord-0f37c9248a30456a9319dc2d4ac67112
出典メモuspto-grants-1989_04