HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1023416Generated: November 3, 2026
Trifluoroacetic acid → HCID 86673604, compound
https://huagongshe.com/reaction/1023416
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-Fluorophenylhydrazine hydrochloride | HCID 69981 | — |
| Reactant | HCID 86673605 | HCID 86673605 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 86673604 | HCID 86673604 | — |
Reaction Steps
(4-Fluoro-phenyl)-hydrazine hydrochloride (95 mg, 0.57 mmol) is dissolved in isopropanol (3.0 mL) and triethylamine (0.08 mL, 0.57 mmol) is added. After the mixture is stirred for 5 min, trifluoroacetic acid (0.09 mL, 1.19 mmol) is added and the mixture is again stirred for 5 min Then 1-(2-Chloro-pyridin-4-yl)-4,4,4-trifluoro-butane-1,3-dione (130 mg, 0.52 mmol) is added and the reaction mixture is heated at 85° C. for 40 hrs and stirred at room temperature for another 48 hrs. Water (20 mL) is added and 1.0 M NaOH solution is used to adjust the pH to about 6. The reaction mixture is then extracted with EtOAc (3×20 ml) and the organic layers are combined and concentrated to give the crude product, which is used without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08722709B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-a858884afd0b44749735fa709bd99a01 |
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| Source note | uspto-grants-2014_05 |
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