HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Fluoro-6-(trifluoromethyl)benzaldehyde → 3-Methyl 5-(1-methylethyl) 2-(fluoromethyl)-4-(2-fluoro-6-(trifluoromethyl)phenyl)-1,4-dihydro-6-methyl-3,5-pyridinedicarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Fluoro-6-(trifluoromethyl)benzaldehyde | HCID 521933 | — |
| Reactant | Isopropyl3-aminocrotonate | HCID 3271821 | — |
| Reactant | Methyl 4-fluoro-3-oxobutanoate | HCID 14170515 | — |
| Product | 3-Methyl 5-(1-methylethyl) 2-(fluoromethyl)-4-(2-fluoro-6-(trifluoromethyl)phenyl)-1,4-dihydro-6-methyl-3,5-pyridinedicarboxylate | HCID 14170534 | 3% |
Reaction Steps
2-Fluoro-6-(trifluoromethyl)benzaldehyde (1.51 g, 7.8 mmoles), methyl 4-fluoro-3-oxobutanoate (1.06 g, 7.8 mmoles) and 1-methylethyl 3-amino-2-butenoate (1.13 g, 7.8 mmoles) were heated at 90° under nitrogen with stirring for 2 hours. The cooled reaction mixture was chromatographed twice; first eluting with toluene/ethyl acetate mixtures and then with ethyl acetate/petroleum ether (60°-80°) mixtures. The title compound (0.1 g) was obtained on evaporation of the pure fractions mp 82°-4°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04686217 |
| Source dataset | uspto-grants-1987_08 |
| ORD ID | ord-bb19e9b64f2446549da75cfab4f3bd94 |
| Source note | uspto-grants-1987_08 |