1-Butanol → Methacrylic acid 1-(n-butoxycarbonyl)-1,1-difluoro-2-butyl ester

HRID 2360534Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2360534
[CH2:1]([OH:5])[CH2:2][CH2:3][CH3:4].C(OC(C)C)(C)C.C(N(CC)CC)C.Cl[C:21]([C:23]([F:34])([F:33])[CH:24]([O:27][C:28](=[O:32])[C:29]([CH3:31])=[CH2:30])[CH2:25][CH3:26])=[O:22]>>[CH2:1]([O:5][C:21]([C:23]([F:33])([F:34])[CH:24]([O:27][C:28](=[O:32])[C:29]([CH3:31])=[CH2:30])[CH2:25][CH3:26])=[O:22])[CH2:2][CH2:3][CH3:4]

Komponenten

5

Edukt 4

HCID 2631-ButanolHCID 7914Diisopropyl EtherHCID 8471TriethylamineHCID 58352381Methacrylic acid 1-chlorocarbonyl-1,1-difluoro-2-butyl ester

Produkt 1

HCID 86663489Methacrylic acid 1-(n-butoxycarbonyl)-1,1-difluoro-2-butyl esterAusbeute 91,1 %

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

Into a 1 L glass flask with a dropping funnel, 62.8 g (0.847 mol, 1.2 eq) of n-butanol, 510 g of diisopropyl ether, 100 g (0.988 mol, 1.4 eq) of triethylamine and 1 g of antioxidant “Nonflex MBP” (manufactured by Seiko Chemical Co., Ltd.) were added. The resulting solution was cooled to 0° C. and stirred, followed by dropping thereto 170 g (purity: 99%, 0.706 mol) of methacrylic acid 1-chlorocarbonyl-1,1-difluoro-2-butyl ester. The thus-obtained reaction solution was stirred for 1 hour at room temperature. The completion of the reaction was confirmed by 19F NMR. The reaction-completed solution was separated into an organic layer and an aqueous layer by the addition of 500 mL of water. The organic layer was dehydrated with magnesium sulfate, filtrated, and then, concentrated under a reduced pressure. The concentration residue was subjected to distillation under a reduced pressure. With this, 179 g of methacrylic acid 1-(n-butoxycarbonyl)-1,1-difluoro-2-butyl ester was obtained as a colorless transparent liquid (yield: 91%, purity: 99%).

Aufarbeitung

  1. addition” (manufactured by Seiko Chemical Co., Ltd.) were added
  2. customThe thus-obtained reaction solution
  3. stirringwas stirred for 1 hour at room temperature
  4. customThe reaction-completed solution was separated into an organic layer
  5. additionan aqueous layer by the addition of 500 mL of water
  6. filtrationfiltrated
  7. concentrationconcentrated under a reduced pressure
  8. distillationThe concentration residue was subjected to distillation under a reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-61770f73d3f64fcdbd3f75849c83f717
Quelldatensatz
uspto-grants-2014_04
Patentnummer
US08686098B2

Notizen zur Reaktion

Wird geladen…