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Hydrochloric Acid → 6-Fluoro-4,4-dimethyl-3,4-dihydroquinolin-2(1H)-one

HRID 1247556
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Reaktionsgleichung

Reaktionsgleichung von HRID 1247556
[F:1][C:2]1[CH:7]=[CH:6][C:5]([NH:8][C:9](=[O:14])[CH:10]=[C:11]([CH3:13])[CH3:12])=[CH:4][CH:3]=1.[Cl-].[Cl-].[Cl-].[Al+3].Cl>C(Cl)(Cl)Cl>[CH3:13][C:11]1([CH3:12])[C:4]2[C:5](=[CH:6][CH:7]=[C:2]([F:1])[CH:3]=2)[NH:8][C:9](=[O:14])[CH2:10]1
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Komponenten

5

Edukt 3

HCID 313Hydrochloric AcidHCID 5320912-Butenamide, N-(4-fluorophenyl)-3-methyl-HCID 6451240Aluminum(III) Chloride

Produkt 1

HCID 219083086-Fluoro-4,4-dimethyl-3,4-dihydroquinolin-2(1H)-one

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6212ChloroformLösungsmittel

Versuchsvorschrift

9.4 g (48.7 mmol) of 3-methyl-2-butenoic acid-(4-fluorophenyl)amide is heated to 130–140° C. and mixed in portions with 9.6 g (73.5 mmol) of aluminum trichloride. After the addition is completed, the temperature is kept at 80° C. for 30 more minutes. It is allowed to cool to room temperature and carefully treated with 60 ml of ice water. After 15.0 ml of chloroform is added, the batch is stirred for 15 minutes, acidified with dilute hydrochloric acid and extracted with chloroform (3×150 ml). The combined organic extracts are washed with saturated NaCl, dried (Na2SO4) and concentrated by evaporation in a vacuum. Column chromatography on silica gel with hexane-ethyl acetate yields 6.0 g.

Aufarbeitung

  1. additionAfter the addition
  2. customis kept at 80° C. for 30 more minutes
  3. extractionextracted with chloroform (3×150 ml)
  4. washThe combined organic extracts are washed with saturated NaCl
  5. dry with materialdried (Na2SO4)
  6. concentrationconcentrated by evaporation in a vacuum
  7. customColumn chromatography on silica gel with hexane-ethyl acetate yields 6.0 g

Quellen und Nachweise

ORD-Eintrag
ord-04158f3bd16d45b29af49e7cb416844d
Quelldatensatz
uspto-grants-2006_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07129270B2

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