Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Pyridinium chloride | HCID 10176127 | — |
| Reactant | HCID 20381196 | HCID 20381196 | — |
| Solvent | Water | HCID 962 | — |
| Product | Pyridinium chloride | HCID 10176127 | — |
| Product | [1,4]Benzodioxino[2,3-b]pyridine | HCID 14294259 | — |
Reaction Steps
Anhydrous pyridine hydrochloride is prepared by distillation to a temperature of 220° C. from a mixture of 42 g of pyridine and 50 ml of concentrated hydrochloric acid. Under a nitrogen atmosphere, the pyridine hydrochloride is allowed to cool to 100° C. and 5 g of 2-chloro-3-(2-methoxyphenoxy)pyridine is added and the mixture is refluxed 1 hour. The mixture is cooled and 200 ml of water is added. The mixture is extracted with 250 ml diethyl ether and the extracts are washed with 10 ml of concentrated ammonium hydroxide. The ether layer is dried and evaporated to yield the pyrido[2,3-B][1,4]benzodioxin, mp 95°-97° C., after sublimation at 0.1 mm pressure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04179506 |
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| Source dataset | uspto-grants-1979_12 |
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| ORD ID | ord-cf66c95b425b49f6b476ab7f78a0ecbb |
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| Source note | uspto-grants-1979_12 |
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