HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 6-Acetyl-4-chloro-3'-fluoro-3-methylbiphenyl-2-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 6-Acetyl-4-chloro-3'-fluoro-3-methylbiphenyl-2-carbonitrile | HCID 58368469 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 6-Acetyl-4-chloro-3'-fluoro-3-methylbiphenyl-2-carboxamide | HCID 86666762 | — |
Reaction Steps
A mixture of 6-acetyl-4-chloro-3′-fluoro-3-methylbiphenyl-2-carbonitrile (0.87 g, 3.0 mmol) and potassium hydroxide (0.34 g, 6.1 mmol) in ethanol (4 mL) was refluxed for 2 hours. The mixture was cooled, acidified with 1 N HCl, and extracted with ethyl acetate. The combined organic layers were washed with brine, dried over magnesium sulfate, and evaporated to dryness under reduced pressure to yield the crude product. LCMS calculated for C16H14ClFNO2 (M+H)+: m/z=306.1. found: 306.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09096600B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-20d449cd2b9846cbaa0a96ccd8340865 |
| Source note | uspto-grants-2015_08 |