Methanol → 4-(2-(diphenylmethoxy)ethyl)-8-hydroxy-3,4-dihydro-2H-1,4-benzoxazine

HRID 2186728Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2186728
C([O:4][C:5]1[C:14]2[O:13][CH2:12][CH2:11][N:10]([CH2:15][CH2:16][O:17][CH:18]([C:25]3[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=3)[C:19]3[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=3)[C:9]=2[CH:8]=[CH:7][CH:6]=1)(=O)C.CO.C(=O)([O-])[O-].[K+].[K+]>C1COCC1>[C:25]1([CH:18]([C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)[O:17][CH2:16][CH2:15][N:10]2[C:9]3[CH:8]=[CH:7][CH:6]=[C:5]([OH:4])[C:14]=3[O:13][CH2:12][CH2:11]2)[CH:26]=[CH:27][CH:28]=[CH:29][CH:30]=1

Komponenten

5

Versuchsvorschrift

8-acetoxy-4-(2-(diphenylmethoxy)ethyl)-3,4-dihydro-2H-1,4-benzoxazine (482 mg) was dissolved in THF (2 ml) and a methanol (10 ml), and anhydrous potassium carbonate (250 mg) was added to the resultant solution, and the mixture was stirred at room temperature for 1 hour. The solvent was distilled off under reduced pressure, and the residue was poured into 5% citric acid, and then extracted with ethyl acetate. The resultant organic layer was washed with water and saturated brine, dried over sodium sulfate, and then concentrated to obtain the colorless oily object compound (429 mg, yield 99%).

Aufarbeitung

  1. distillationThe solvent was distilled off under reduced pressure
  2. additionthe residue was poured into 5% citric acid
  3. extractionextracted with ethyl acetate
  4. washThe resultant organic layer was washed with water and saturated brine
  5. dry with materialdried over sodium sulfate
  6. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-14cb420f5fee40cd9eea772f15b7fbed
Quelldatensatz
uspto-grants-2002_06
Patentnummer
US06407096B1

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