Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Aminobenzophenone | HCID 76080 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2'-Benzoylacetanilide | HCID 97474 | — |
| Product | 2-Chloro-4-phenylquinoline | HCID 2306687 | — |
Reaction Steps
2-Chloro-4-phenylquinoline was prepared by the following method (Rxn-1). 2-Aminobenzophenone (21 g, 106.5 mmol) was dissolved in methylene chloride (213 mL) and triethylamine (22.3 mL, 159.8 mmol) was added slowly. After cooling to 0° C., acetylchloride (8.3 mL, 117.2 mmol) was added to the reaction mixture dropwise. The reaction mixture was then removed from ice and allowed to stir overnight. Upon the addition of 10% hydrochloric acid (84 mL), the aqueous layers were combined and extracted with ethyl acetate. The organic phases were combined, dried with magnesium sulfate, and concentrated. Purification by column chromatography (25% ethyl acetate/heptane) gave 2-acetamidobenzophenone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07070868B2 |
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| Source dataset | uspto-grants-2006_07 |
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| ORD ID | ord-587fa6dd1dba43fda10d118c83fddfdf |
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| Source note | uspto-grants-2006_07 |
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