Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 3-Methyl-2-butanone | HCID 11251 | — |
| Reactant | 4-Fluoro-3-phenoxybenzaldehyde | HCID 110068 | — |
| Reactant | Ethyl 5-methyl-4-oxohexanoate | HCID 12892835 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 54092388 | HCID 54092388 | — |
Reaction Steps
2.8 ml (29 mmol) of piperidine and 1.7 ml (29 mmol) of acetic acid are added to a solution of 79 g (0.5 mol) of ethyl 4-methyl-3-oxo-pentanecarboxylate (prepared from methyl isopropyl ketone analogously to the process of S. B. Soloway and F. B. La Forge, J. Am. Chem. Soc. 69, 2677 (1947)) and 108 g (0.5 mol) of 4-fluoro-3-phenoxy-benzaldehyde in 300 ml of isopropanol and stirred overnight at RT. The mixture is then concentrated, the residue is taken up in 500 ml of ether, washed twice with water and once with saturated sodium chloride solution, dried over sodium sulphate and the solvent removed. The residue is distilled under high vacuum until the last fraction passes over at 185° C. and 0.3 mbar. All distillates (44 g) are discarded. The distillation residue contains the product: brownish oil (144.7 g, 81%), which is reacted further without purification. Rf =0.25 (petroleum ether/ethyl acetate 10:1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05032590 |
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| Source dataset | uspto-grants-1991_07 |
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| ORD ID | ord-e2bd23c1acb14d04acb9dbdf3a9a86fe |
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| Source note | uspto-grants-1991_07 |
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