Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Hydrogen iodide | HCID 24841 | — |
| Reactant | 1,3-Dichloroisoquinoline | HCID 298625 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 3-Chloroisoquinoline | HCID 640968 | — |
Reaction Steps
A mixture of 1,3-dichloroisoquinoline (26.0 g; prepared according to the method of G Simchen, Angew. Chem. Internat. Ed. 5 (7), 663, 1966), acetic acid (125 ml), hydrogen iodide (55 ml) and red phosphorus (9.0 g) was heated with stirring at a temperature of 170° C. for a period of 3 hours. After cooling the mixture was poured into ice-water and the aqueous mixture was neutralized with aqueous sodium hydroxide. The aqueous mixture was extracted with dichloromethane and the organic extract was dried over anhydrous magnesium sulfate. The solvent was evaporated to give an oil which was purified by column chromatography over silica gel (eluant dichloromethane) to give 3-chloroisoquinoline (18.23 g) mp<50° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04409017 |
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| Source dataset | uspto-grants-1983_10 |
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| ORD ID | ord-c0053f28893d40fc8672f9d1eee232be |
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| Source note | uspto-grants-1983_10 |
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