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1,1-Dibromoethane → 2H-1,4-Benzoxazine, 3,4-dihydro-4-methyl-

HRID 970318
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 970318
[CH3:1][NH:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[OH:9].Br[CH:11](Br)[CH3:12].C(=O)([O-])[O-].[K+].[K+]>CC(C)=O.O>[CH3:1][N:2]1[C:3]2[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=2[O:9][CH2:12][CH2:11]1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 3

HCID 112011,1-DibromoethaneHCID 11430Potassium CarbonateHCID 69138o-(Methylamino)phenol

Produkt 1

HCID 37550242H-1,4-Benzoxazine, 3,4-dihydro-4-methyl-Ausbeute 79 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 180AcetoneLösungsmittelHCID 962
Water
Lösungsmittel

Versuchsvorschrift

To a mixture of 104A (2.33 g, 18.9 mmol) and dibromoethane (6.5 mL, 75.7 mmol) in a mixture of acetone (80 mL) and water (20 mL) at room temperature was added potassium carbonate (10.46 g, 75.7 mmol). The mixture was heated at reflux for 3 days. HPLC indicated that the reaction was complete, and the acetone was removed under reduced pressure. The aqueous residue was extracted with DCM, washed with water, and dried over anhydrous sodium sulfate. Concentration under reduced pressure followed by purification by silica gel chromatography afforded 104B (2.22 g, 79%). HPLC retention time=2.07 min. (Condition B) and LC/MS M+1=150.08. 1H-NMR (500 MHz, CDCl3) δ 2.91 (s, 3H), 3.28 (t, 2H), 4.33 (t, 2H), 6.70 (t, 1H, J=7.5 Hz), 6.72 (d, 1H, J=7.5 Hz), 6.82 (d, 1H, J=7.5 Hz), and 6.89 (t, 1H, J=7.5 Hz).

Aufarbeitung

  1. temperatureThe mixture was heated
  2. temperatureat reflux for 3 days
  3. customthe acetone was removed under reduced pressure
  4. extractionThe aqueous residue was extracted with DCM
  5. washwashed with water
  6. dry with materialdried over anhydrous sodium sulfate
  7. concentrationConcentration under reduced pressure
  8. customfollowed by purification by silica gel chromatography

Quellen und Nachweise

ORD-Eintrag
ord-95b64d6cec094887a8203eb207abaaa8
Quelldatensatz
uspto-grants-2007_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07312209B2

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