p-Toluenesulfonic acid monohydrate → 7-Bromo-2-tert-butyl-5-methyl-6-styryl-1,3-benzoxazole-4-carbonitrile

HRID 17277

Reaktionsgleichung

Reaktionsgleichung von HRID 17277
O.C1(C)C=CC(S(O)(=O)=O)=CC=1.[Br:13][C:14]1[C:15](O)=[C:16]([NH:31][C:32](=[O:37])[C:33]([CH3:36])([CH3:35])[CH3:34])[C:17]([C:29]#[N:30])=[C:18]([CH3:28])[C:19]=1[CH:20]=[CH:21][C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1.O.C(=O)(O)[O-].[Na+]>C1(C)C=CC=CC=1>[Br:13][C:14]1[C:19]([CH:20]=[CH:21][C:22]2[CH:23]=[CH:24][CH:25]=[CH:26][CH:27]=2)=[C:18]([CH3:28])[C:17]([C:29]#[N:30])=[C:16]2[C:15]=1[O:37][C:32]([C:33]([CH3:36])([CH3:35])[CH3:34])=[N:31]2

Komponenten

5

Edukt 3

HCID 521998p-Toluenesulfonic acid monohydrateHCID 86585896Sodium bicarbonate waterHCID 86630801N-(3-Bromo-6-cyano-2-hydroxy-5-methyl-4-styrylphenyl)-2,2-dimethylpropionamide

Produkt 1

HCID 685840107-Bromo-2-tert-butyl-5-methyl-6-styryl-1,3-benzoxazole-4-carbonitrileAusbeute 84,3 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 1140TolueneLösungsmittel

Versuchsvorschrift

Toluene (3 ml), p-toluenesulfonic acid monohydrate (1.4 mg, 7.5 μmol) were added to N-(3-bromo-6-cyano-2-hydroxy-5-methyl-4-styrylphenyl)-2,2-dimethylpropionamide (I-14) (31 mg, 75 μmol), followed by refluxing with a Dean-Stark condenser for 2.5 hours. After cooling, saturated sodium bicarbonate water (30 ml) was added to the reaction liquid, the product was extracted with ethyl acetate (30 ml×2). The organic layer was washed with saturated brine (30 ml), dried over anhydrous magnesium sulfate, concentrated under reduced pressure, the residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=8:1) to obtain the entitled compound (25 mg, 84%) as a colorless solid.

Aufarbeitung

  1. temperatureby refluxing with a Dean-Stark condenser for 2.5 hours
  2. temperatureAfter cooling
  3. extractionthe product was extracted with ethyl acetate (30 ml×2)
  4. washThe organic layer was washed with saturated brine (30 ml)
  5. dry with materialdried over anhydrous magnesium sulfate
  6. concentrationconcentrated under reduced pressure
  7. customthe residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=8:1)

Quellen und Nachweise

ORD-Eintrag
ord-ff74efec60a34a189d6388ef3f692111
Quelldatensatz
uspto-grants-2010_06
Patentnummer
US07737166B2

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