1,4-Dioxane → Methyl 3-dimethylamino-2-(2,3,4,5-tetrafluorobenzoyl)acrylate

HRID 1708543

Reaktionsgleichung

Reaktionsgleichung von HRID 1708543
O1CCOCC1.[F:7][C:8]1[C:16]([F:17])=[C:15]([F:18])[C:14]([F:19])=[CH:13][C:9]=1[C:10](Cl)=[O:11].[CH3:20][N:21]([CH3:28])[CH:22]=[CH:23][C:24]([O:26][CH3:27])=[O:25]>C(N(CC)CC)C>[CH3:20][N:21]([CH3:28])[CH:22]=[C:23]([C:10](=[O:11])[C:9]1[CH:13]=[C:14]([F:19])[C:15]([F:18])=[C:16]([F:17])[C:8]=1[F:7])[C:24]([O:26][CH3:27])=[O:25]

Komponenten

5

Edukt 3

HCID 312751,4-Dioxane2×HCID 566587Methyl 3-(dimethylamino)acrylateHCID 27336892,3,4,5-Tetrafluorobenzoyl chloride

Produkt 1

HCID 53884844Methyl 3-dimethylamino-2-(2,3,4,5-tetrafluorobenzoyl)acrylateAusbeute 50,7 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8471TriethylamineLösungsmittel

Versuchsvorschrift

To dioxane (80 ml) solution of 2,3,4,5-tetrafluorobenzoyl chloride (21.25 g) was added dioxane (25 ml) solution of methyl 3-dimethylaminoacrylate (12.92 g) with ice-cooling, and triethylamine (14.46 ml) was added thereto with ice-cooling. The mixture was stirred for 30 minutes at the same temperature, then for 3 hours at room temperature, and then for one hour at 50° to 60° C. The mixture was concentrated under reduced pressure, then dissolved in methylene chloride (200 ml), washed with water (200 ml) and brine (100 ml) in order, then dried with sodium sulfate and concentrated under reduced pressure to obtain a syrup product. The syrup product was subjected to column chromatography with silica gel and eluted with a mixed liquid of methanol/methylene chloride (3/97, V/V) to obtain methyl 3-dimethylamino-2-(2,3,4,5-tetrafluorobenzoyl)acrylate (15.47 g) as a syrup product.

Aufarbeitung

  1. temperaturecooling
  2. temperaturewith ice-cooling
  3. waitfor 3 hours at room temperature
  4. waitfor one hour at 50° to 60° C
  5. concentrationThe mixture was concentrated under reduced pressure
  6. dissolutiondissolved in methylene chloride (200 ml)
  7. washwashed with water (200 ml) and brine (100 ml) in order
  8. dry with materialdried with sodium sulfate
  9. concentrationconcentrated under reduced pressure
  10. customto obtain a syrup product
  11. washeluted with a mixed liquid of methanol/methylene chloride (3/97, V/V)

Quellen und Nachweise

ORD-Eintrag
ord-fccdf0d855e94d9ca6306e5392f57271
Quelldatensatz
uspto-grants-1994_10
Patentnummer
US05359066

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