Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Diethyl Malonate | HCID 7761 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | HCID 21467573 | HCID 21467573 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 21467568 | HCID 21467568 | — |
Reaction Steps
To 460 mg of 1-(4-methoxybenzyl)-2-chloroindole-carbaldehyde, dissolved in 15 ml of a solvent which consisted of 5% piperidine and 2% acetic acid in absolute ethanol, was added 0.26 ml of diethyl malonate. After stirring for 3 days the solvent was removed by evaporation, and the product dissolved in 25 ml of ether plus 25 ml of 1N HCl. The organic phase was separated, and washed with 25 ml 1 N HCl, 25 ml water, 25 ml of saturated NaHCO3 solution, dried (MgSO4) and evaporated to give an oil. Purification by column chromatography (methylene chloride on silica 60) gave (15a) as an oil. 1H-NMR (CDCl3): 8.03 (s, 1H); 7.50 (m, 1H); 7.20 (m, 3H); 7.02 (d, 2H); 6.78 (d, 2H); 5.30 (s, 2H); 4.32 (q, 2H); 4.24 (q, 2H); 3.71 (s, 3H); 1.33 (t, 3H) 1.11 (t, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05696148 |
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| Source dataset | uspto-grants-1997_12 |
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| ORD ID | ord-aff339c842fb4975a9026e72cc8fa94b |
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| Source note | uspto-grants-1997_12 |
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