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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | 4-(Dimethylamino)benzophenone | HCID 10737 | — |
| Reactant | 2-Trimethylsilyl-1,3-dithiane | HCID 83413 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 4-[(1,3-Dithian-2-ylidene)(phenyl)methyl]-N,N-dimethylaniline | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04946861 |
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| Source dataset | uspto-grants-1990_08 |
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| ORD ID | ord-46024b1f7ed94f84adbec3203a3b2645 |
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| Source note | uspto-grants-1990_08 |
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