HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1076267Generated: October 25, 2026
Dimethylformamide → 1,3,5-Tricarbethoxy-1,4-dihydro-2,6-dimethyl-4-(2-trifluoromethylphenyl)pyridine
https://huagongshe.com/reaction/1076267
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1,4-Dihydro-2,6-dimethyl-4-(2-(trifluoromethyl)phenyl)-3,5-pyridinedicarboxylic acid diethyl ester | HCID 168089 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1,3,5-Tricarbethoxy-1,4-dihydro-2,6-dimethyl-4-(2-trifluoromethylphenyl)pyridine | HCID 12196458 | — |
Reaction Steps
To 1.2 g. of sodium hydride (57% dispersion in mineral oil) suspended in tetrahydrofuran is added dropwise with stirring a solution of 10 g. of 3,5-dicarbethoxy-1,4-dihydro-2,6-dimethyl-4-(2-trifluoromethylphenyl)pyridine in tetrahydrofuran. The mixture is heated on a steam bath for 15 minutes, then it is cooled and enough dimethylformamide is added to dissolve the solid which has separated. To the resulting solution is added dropwise 3.04 g. of ethyl chloroformate and the reaction mixture is stirred at 25° for 15 minutes then heated on a steam bath for 12 hours. The mixture is filtered and concentrated to give an oil which is dissolved in acetonitrile. The solution is extracted with petroleum ether then concentrated to give an oil which is stirred with petroleum ether. The solid formed is filtered and the filtrate is concentrated in vacuo to give an oil which is chromatographed on an alumina "dry column" with methylene chloride as eluant to give 1,3,5-tricarbethoxy-1,4-dihydro-2,6-dimethyl-4-(2-trifluoromethylphenyl)pyridine, m.p. 56°-58°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03956341 |
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| Source dataset | uspto-grants-1976_05 |
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| ORD ID | ord-2bd16385e24446f3a227dd5827eb0e7a |
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| Source note | uspto-grants-1976_05 |
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