HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 245244Erstellt: 24. Oktober 2026
5-Bromoisatin → 6-Bromo-3-methyl-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylic acid
https://huagongshe.com/de/reaction/245244
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 5-Bromoisatin | HCID 6889 | — |
| Edukt | Potassium Hydroxide | HCID 14797 | — |
| Edukt | Propiophenone, 3'-(trifluoromethyl) | HCID 137064 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 6-Bromo-3-methyl-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylic acid | HCID 67383995 | 116,4% |
Reaktionsschritte
Potassium hydroxide (29.8 g, 531 mmol) in water (49.2 mL) was added to an orange suspension of 5-bromoisatin (20 g, 88 mmol) in ethanol (172 mL). 1-[3-(Trifluoromethyl)phenyl]-1-propanone (19.68 g, 97 mmol) was added and the mixture was heated to 85° C. for 3 h. The solvent was removed under reduced pressure. The residue was diluted with water (400 mL) and stirred overnight. The aqueous mixture was cooled to 0° C. and adjusted to pH˜3 with concentrated HCl. The solid was collected by filtration and dried in a vacuum oven at 70° C. for 3 days to afford 6-bromo-3-methyl-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylic acid (42 g, >99% yield). This material was used without further purification. MS (m/z) 411.8 (M+H+).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08658636B2 |
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| Quelldatensatz | uspto-grants-2014_02 |
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| ORD ID | ord-c3533996947e4490825591d436c4c31f |
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| Quellennotiz | uspto-grants-2014_02 |
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