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HRID 620063생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/620063

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물4-(Dimethylamino)benzophenoneHCID 10737—
반응물2-Trimethylsilyl-1,3-dithianeHCID 83413—
반응물ButyllithiumHCID 178418339—
용매DichloromethaneHCID 6344—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물4-[(1,3-Dithian-2-ylidene)(phenyl)methyl]-N,N-dimethylanilineHCID 13301997—

반응 단계

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°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04818765
출처 데이터셋uspto-grants-1989_04
ORD IDord-81be7c86c7d84239b7b61676fc535fd3
출처 메모uspto-grants-1989_04