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HRID 1708997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/1708997

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 (1000 ml ) and dichloromethane (200 ml). After separation of the layers, the aqueous solution is extracted with dichloromethane (3×200 ml). The combined organic solutions are 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US04946861
出典データセットuspto-grants-1990_08
ORD IDord-46024b1f7ed94f84adbec3203a3b2645
出典メモuspto-grants-1990_08