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Phosphorus oxychloride → 2,2-dimethyl-4-chloro-6-cyano-2H-1,3-benzoxazine

HRID 326579
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 326579
P(Cl)(Cl)([Cl:3])=O.[C:6]([C:8]1[CH:9]=[CH:10][C:11]2[O:16][C:15]([CH3:18])([CH3:17])[NH:14][C:13](=O)[C:12]=2[CH:20]=1)#[N:7]>CN(C)C=O>[Cl:3][C:13]1[C:12]2[CH:20]=[C:8]([C:6]#[N:7])[CH:9]=[CH:10][C:11]=2[O:16][C:15]([CH3:18])([CH3:17])[N:14]=1
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Komponenten

4

Edukt 2

HCID 24813Phosphorus oxychlorideHCID 108219722,2-dimethyl-6-cyano-3,4-dihydro-2H-1,3-benzoxazin-4-one

Produkt 1

HCID 147215882,2-dimethyl-4-chloro-6-cyano-2H-1,3-benzoxazine

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideLösungsmittel

Versuchsvorschrift

Phosphorous oxychloride (0.5 ml) was added with ice-cooling to dimethylformamide (10 ml) and the mixture was stirred for 10 minutes. To the mixture was added 6-cyano-2,2-dimethyl-3,4-dihydro-2H-1,3-benzoxazin-4-one (1.0 g), and the mixture was stirred with ice-cooling for 1 hour and then at room temperature for 2 hours. The mixture was extracted with addition of ethyl acetate and ice water. The ethyl acetate layer was successively washed with an aqueous sodium bicarbonate solution and saturated saline, dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure. Hexane was added to the residue and 4-chloro-6-cyano-2,2-dimethyl-2H-1,3-benzoxazine (0.41 g, mp. 124°-126° C.) was obtained by crystallization therefrom.

Aufarbeitung

  1. stirringthe mixture was stirred with ice-
  2. temperaturecooling for 1 hour
  3. waitat room temperature for 2 hours
  4. extractionThe mixture was extracted with addition of ethyl acetate and ice water
  5. washThe ethyl acetate layer was successively washed with an aqueous sodium bicarbonate solution and saturated saline
  6. dry with materialdried over anhydrous magnesium sulfate
  7. distillationThe solvent was distilled off under reduced pressure
  8. additionHexane was added to the residue

Quellen und Nachweise

ORD-Eintrag
ord-59f07b0f946f4f9e8d5e7ab10ad12c4b
Quelldatensatz
uspto-grants-1993_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05270308

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