Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosgene | HCID 6371 | — |
| Reactant | HCID 11423781 | HCID 11423781 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 20477505 | HCID 20477505 | — |
Reaction Steps
33.0 parts of 6-fluoro-4-oxo-1,2,3,4-tetrahydroquinoline and 200 parts of dioxane were mixed, and 39.6 parts of phosgene were introduced to the stirred mixture over about 30 minutes while the temperature was maintained at 20°-25° C. After the introduction, the temperature was raised gradually, and the reaction was effected at 40°-45° C. for 2.5 hours, after which the temperature was further raised to 70° C., nitrogen gas was passed through the mixture, and the solvent (dioxane) was distilled off under reduced pressure. Petroleum ether was added to the residue followed by filtration, washing and drying, and there was obtained 43.7 parts of 6-fluoro-4-oxo-1-chloroformyl-1,2,3,4-tetrahydroquinoline.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04421919 |
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| Source dataset | uspto-grants-1983_12 |
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| ORD ID | ord-3fa4c40de51f4659b924a845b3d8b5b8 |
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| Source note | uspto-grants-1983_12 |
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