Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cinchophen | HCID 8593 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Phenylquinoline-4-carbonyl chloride | HCID 2760409 | — |
Reaction Steps
11.7 ml (136.3 mmol) of oxalyl chloride were dissolved in 150 ml of CH2Cl2. The solution was cooled at −10° C. and 20 g (80.2 mmol) of commercially available 2-phenylquinoline-4-carboxylic acid were added portionwise. The reaction mixture was left overnight at room temperature and then evaporated to dryness to yield 22 g of the title compound, used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06743804B2 |
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| Source dataset | uspto-grants-2004_06 |
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| ORD ID | ord-b95427c06ebb4f998a8b420b3a9d9781 |
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| Source note | uspto-grants-2004_06 |
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