Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Ethylene Oxide | HCID 6354 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Potassium | HCID 5462222 | — |
| Reactant | HCID 21411769 | HCID 21411769 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 21411766 | HCID 21411766 | 70% |
Reaction Steps
To stirred liquid ammonia (2 liters) was added ferric nitrate (0.1 gm) followed by potassium metal (14 gms) in 1 gram pieces over a period of 20 minutes. To the resulting solution 3-(4-pyridyl)-propionaldehyde diethyl acetal (21 gms) was added over a period of 3 minutes and a deep yellow colour was allowed to develop over a period of 2 hours. Liquid ethylene oxide (25 mls) was then added and the mixture was stirred for a further 3 hours. Solid ammonium chloride (20 gms) was added in small portions followed by diethyl ether (1 liter). The ammonia was allowed to evaporate overnight and the residual mixture was filtered. The solvent was evaporated from the filtrate and the residual oil was distilled to give 1,1-diethoxy-3-(4-pyridyl)-pentan-5-ol (18 gms, 70% conversion) b.p. 170°-175° C/1 mm Hg, as a thick colourless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04048180 |
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| Source dataset | uspto-grants-1977_09 |
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| ORD ID | ord-cb329e49a81741caac8dbf74f0f328e4 |
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| Source note | uspto-grants-1977_09 |
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