Hydroxyamine hydrochloride → 4-(3,5-Dimethyl-pyridin-4-yl)-3,5-dimethyl-phenylamine

HRID 2425831Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2425831
[CH3:1][C:2]1[CH:3]=[N:4][CH:5]=[C:6]([CH3:30])[C:7]=1[C:8]1[C:13]([CH3:14])=[CH:12][C:11]([N:15]=C(C2C=CC=CC=2)C2C=CC=CC=2)=[CH:10][C:9]=1[CH3:29].CC([O-])=O.[Na+].Cl.NO>CO>[CH3:1][C:2]1[CH:3]=[N:4][CH:5]=[C:6]([CH3:30])[C:7]=1[C:8]1[C:13]([CH3:14])=[CH:12][C:11]([NH2:15])=[CH:10][C:9]=1[CH3:29]

Komponenten

5

Edukt 3

HCID 443297Hydroxyamine hydrochlorideHCID 517045Sodium AcetateHCID 595503324-(3,5-dimethylpyridin-4-yl)-N-(diphenylmethylene)-3,5-dimethyl-benzenamine

Produkt 1

HCID 595503394-(3,5-Dimethyl-pyridin-4-yl)-3,5-dimethyl-phenylamineAusbeute 99 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 887MethanolLösungsmittel

Versuchsvorschrift

To a solution of 9 (0.36 g, 0.93 mmol) in anhydrous MeOH (10 mL) at room temperature was added with stirring NaOAc (0.197 g, 2.40 mmol) and hydroxylamine hydrochloride (0.125 g, 1.80 mmol). The reaction mixture was then stirred at room temperature for 1.5 h. The resulting solution was next partitioned between an aqueous 0.1 M NaOH solution (50 mL) and CH2Cl2 (50 mL×3). The organic layer was separated, dried over anhydrous Na2SO4, filtered, and concentrated in vacuo. The crude product was next purified by flash chromatography on silica gel, eluting with ethyl acetate, to give 0.207 g (99.0%) of the title compound as yellow solid: mp 134-135° C.; 1H NMR (400 MHz, CD2Cl2): δ 8.311 (s, 2H), 6.482 (s, 2H), 1.903 (s, 6H), 1.769 (s, 6H); 13C NMR (100 MHz, CD2Cl2): δ 149.130, 148.547, 146.482, 135.882, 132.333, 127.592, 114.635, 19.979, 16.876; MS (ESI): m/z 227.5 [(M+H)+, 100]; Anal. Calcd. for C15H18N2: C, 79.61; H, 8.02; N, 12.38. Found; C, 79.26; H, 7.91; N, 12.04.

Aufarbeitung

  1. customThe resulting solution was next partitioned between an aqueous 0.1 M NaOH solution (50 mL) and CH2Cl2 (50 mL×3)
  2. customThe organic layer was separated
  3. dry with materialdried over anhydrous Na2SO4
  4. filtrationfiltered
  5. concentrationconcentrated in vacuo
  6. customThe crude product was next purified by flash chromatography on silica gel
  7. washeluting with ethyl acetate

Quellen und Nachweise

ORD-Eintrag
ord-3df06844ed4a414197d4be253b7d1948
Quelldatensatz
uspto-grants-2011_06
Patentnummer
US07968016B2

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