Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 4-Bromophenylhydrazine hydrochloride | HCID 12157 | — |
| Reactant | HCID 131735955 | HCID 131735955 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 118431647 | HCID 118431647 | 89.2% |
Reaction Steps
1-(2,4-Difluoro-phenyl)-4,4,5,5,5-pentafluoro-pent-1-en-3-one (3.8 g, 13.3 mmol) prepared in Step 3 of Preparation 14, 4-bromophenylhydrazine hydrochloride (3.3 g, 13.5 mmol), acetic acid (15.0 mL) and conc. hydrochloric acid (20.0 mL) were added to ethanol (35.0 mL). The reaction mixture was stirred at 100° C. for 18 hours, quenched with a saturated solution of sodium hydrogen carbonate, and then extracted with ethyl acetate three times. The combined extract was washed with brine, dried on anhydrous magnesium sulfate, and then concentrated under reduced pressure to give a yellow liquid residue. The resulting residue was purified by silica gel column chromatography (eluent: ethyl acetate/n-hexane=1/10) to give 5.4 g of the titled compound as a yellow liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09376420B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-f08b8da824824ba7b50c8c5248920b40 |
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| Source note | uspto-grants-2016_06 |
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