Hydrochloric Acid → 2-Fluoro-3-(3-fluorophenyl)-5-methoxybenzoic acid

HRID 1771611Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1771611
[F:1][C:2]1[C:10](I)=[CH:9][C:8]([O:12][CH3:13])=[CH:7][C:3]=1[C:4]([OH:6])=[O:5].[F:14][C:15]1[CH:16]=[C:17](B(O)O)[CH:18]=[CH:19][CH:20]=1.C([O-])([O-])=O.[Na+].[Na+].Cl>O.C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.CN(C=O)C.CCO>[F:1][C:2]1[C:10]([C:19]2[CH:18]=[CH:17][CH:16]=[C:15]([F:14])[CH:20]=2)=[CH:9][C:8]([O:12][CH3:13])=[CH:7][C:3]=1[C:4]([OH:6])=[O:5]

Komponenten

9

Edukt 4

HCID 313Hydrochloric AcidHCID 10340Sodium CarbonateHCID 27339863-Fluorophenylboronic acidHCID 894441282-Fluoro-3-iodo-5-methoxybenzoic acid

Produkt 1

HCID 894438332-Fluoro-3-(3-fluorophenyl)-5-methoxybenzoic acidAusbeute 82,1 %

Reagenzien, Katalysatoren, Lösungsmittel 4

HCID 178418397HCID 178418397, VerbindungKatalysatorHCID 702EthanolLösungsmittelHCID 962WaterLösungsmittelHCID 6228DimethylformamideLösungsmittel

Versuchsvorschrift

To a solution of 2-fluoro-3-iodo-5-methoxy-benzoic acid (3.0 g 10.14 mmol, 1.0 eq) in a mixture of water (30 mL), EtOH (30 mL) and DMF (60 mL), was added 3-fluorophenylboronic acid (1.56 g 11.15 mmol, 1.1 eq) and Na2CO3 (4.3 g, 40.56 mmol, 4.0 eq). The mixture was stirred at room temperature under N2 for 10 mins then Pd(PPh3)4 (1.17 g, 1.01 mmol, 0.1 eq) was added. The mixture was heated at 100° C. for 5 h then cooled to room temperature and acidified with 1M HCl. The aqueous layer was extracted with EtOAc and the combined extracts were washed with water, dried (Na2SO4), filtered and evaporated in vacuo. The residue was purified by column chromatography (EtOAc:petroleum ether, 0:1 to 1:3) to give the title compound as a yellow solid (2.2 g, 81%).

Aufarbeitung

  1. temperatureThe mixture was heated at 100° C. for 5 h
  2. temperaturethen cooled to room temperature
  3. extractionThe aqueous layer was extracted with EtOAc
  4. washthe combined extracts were washed with water
  5. dry with materialdried (Na2SO4)
  6. filtrationfiltered
  7. customevaporated in vacuo
  8. customThe residue was purified by column chromatography (EtOAc:petroleum ether, 0:1 to 1:3)

Quellen und Nachweise

ORD-Eintrag
ord-8bf0f5eec2e0485c8c96fb2656efb925
Quelldatensatz
uspto-grants-2016_02
Patentnummer
US09249085B2

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