Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | o-(Trifluoromethyl)benzaldehyde | HCID 123067 | — |
| Reactant | Benzyl acetoacetate | HCID 142266 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 19009986 | HCID 19009986 | 76% |
Reaction Steps
In a 7% ammonia solution in methanol were dissolved 2.6 g of o-trifluoromethylbenzaldehyde and 5.8 g of benzyl acetoacetate, and the solution was stirred in a closed tube at 90° C. for 10 hours. The reaction mxiture was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (methanol/dichloromethane =1/50) to obtain 6.0 g (yield: 76%) of dibenzyl 1,4-dihydro -2,6-dimethyl-4-(2-trifluoromethylphenyl)-3,5-pyridinedicarboxylate as a yellow oily substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05234821 |
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| Source dataset | uspto-grants-1993_08 |
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| ORD ID | ord-ad4ac61aaa5d47c19307b5afa797ccb6 |
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| Source note | uspto-grants-1993_08 |
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