Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Nitrate | HCID 24434 | — |
| Reactant | HCID 12802705 | HCID 12802705 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | HCID 12802770 | HCID 12802770 | 85% |
Reaction Steps
1-(4-Chlorobenzyl)-1,2-dihydro-2-oxoquinol-4-ylacetic acid (33 g.) was added to concentrated sulphuric acid (210 ml.) at 0° C. The mixture was stirred at 0° C. and potassium nitrate (11 g.) was added in small portions over 8 minutes. The mixture was then stirred at 0° C. for a further 10 minutes and then for 2 hours at room temperature. The mixture was poured into an ice-water mixture (2.5 l.), and the precipitated solid was filtered off. The dried solid was crystallised from 3/1 v/v dimethylformamide-ethanol to give 1-(4-chlorobenzyl)-1,2-dihydro-6-nitro-2-oxoquinol-4-ylacetic acid, m.p. 217°-9° C., in 85% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04187310 |
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| Source dataset | uspto-grants-1980_02 |
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| ORD ID | ord-ed4404b29f224f71ac5b783741dc4894 |
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| Source note | uspto-grants-1980_02 |
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