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HRID 620063作成日:2026年10月26日

Water → 4-[(1,3-Dithian-2-ylidene)(phenyl)methyl]-N,N-dimethylaniline

https://huagongshe.com/reaction/620063

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物4-(Dimethylamino)benzophenoneHCID 10737—
反応物2-Trimethylsilyl-1,3-dithianeHCID 83413—
反応物ButyllithiumHCID 178418339—
溶媒DichloromethaneHCID 6344—
溶媒TetrahydrofuranHCID 8028—
溶媒HexaneHCID 8058—
生成物4-[(1,3-Dithian-2-ylidene)(phenyl)methyl]-N,N-dimethylanilineHCID 13301997—

反応手順

There is added to a solution of 2-trimethylsilyl-1,3-dithiane (16.2 g) in dry tetrahydrofuran (170 ml) at -65° a 1.9M solution of n-butyllithium in hexane (45 ml). The reaction mixture is progressively warmed to 0° in the course of 31/2 hours and cooled to -65°. A solution of 4-dimethylamino-benzophenone (19.2 g) in dry tetrahydrofuran (100 ml) is than slowly added. The reaction mixture is progressively warmed to room temperature overnight and poured into a mixture of water (1000ml) and dichloromethane (200 ml). After separation of the layers, the aqueous solution is extracted with dichloromethane (3×200 ml). The combined organic solutions was washed with water (100 ml) and dried over magnesium sulphate. The solvents are evaporated in vacuo and the residue is recrystallised from ethyl acetate. The product is dried in vacuo to constant weight to yield (4-dimethylaminophenyl)-(1,3-dithian-2-ylidene)-phenylmethane, m.p. 172°-174°.

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-81be7c86c7d84239b7b61676fc535fd3
出典メモuspto-grants-1989_04