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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1708997Generated: October 26, 2026

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

https://huagongshe.com/reaction/1708997

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-(Dimethylamino)benzophenoneHCID 10737—
Reactant2-Trimethylsilyl-1,3-dithianeHCID 83413—
ReactantButyllithiumHCID 178418339—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product4-[(1,3-Dithian-2-ylidene)(phenyl)methyl]-N,N-dimethylanilineHCID 13301997—

Reaction Steps

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°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04946861
Source datasetuspto-grants-1990_08
ORD IDord-46024b1f7ed94f84adbec3203a3b2645
Source noteuspto-grants-1990_08