Ammonia → 2-Amino-3-bromo-6,7-dimethylnaphthalene-1,4-dione

HRID 444229Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 444229
[NH3:1].[Br:2][C:3]1[C:4](=[O:17])[C:5]2[C:10]([C:11](=[O:14])[C:12]=1Br)=[CH:9][C:8]([CH3:15])=[C:7]([CH3:16])[CH:6]=2>[N+](C1C=CC=CC=1)([O-])=O>[NH2:1][C:12]1[C:11](=[O:14])[C:10]2[C:5]([C:4](=[O:17])[C:3]=1[Br:2])=[CH:6][C:7]([CH3:16])=[C:8]([CH3:15])[CH:9]=2

Komponenten

4

Edukt 2

HCID 222AmmoniaHCID 2463472,3-Dibromo-6,7-dimethylnaphthalene-1,4-dione

Produkt 1

HCID 2463482-Amino-3-bromo-6,7-dimethylnaphthalene-1,4-dioneAusbeute 86 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 7416NitrobenzeneLösungsmittel

Versuchsvorschrift

Dry ammonia was passed through a refluxing solution of 2,3-dibromo-6,7-dimethyl-1,4-naphthoquinone (10 g; mp 237°-238° C.) in dry nitrobenzene (65 ml) for 30 mins. and the orange solid which separated on cooling was filtered off and washed with light petroleum. After removal of ammonium bromide with water, 6.96 g. (86%) of material of mp 228° C. was obtained. Recrystallisation from glacial acetic acid gave analytically pure material of the same melting point. ν max(mull) 3400, 3300, 1680, 1610, 1585, 1570 cm-1. δ(DMSO) 2.35 (6H,s); 7.35 (2H, exchangeable broad singlet); 7.74 (2H,s). (Found; C, 51.50; H, 3.38; N, 4.79; C12H10BrNO2 requires; C, 51.45; H, 3.60; N, 5.00%).

Aufarbeitung

  1. customand the orange solid which separated
  2. temperatureon cooling
  3. filtrationwas filtered off
  4. washwashed with light petroleum
  5. customAfter removal of ammonium bromide with water, 6.96 g

Quellen und Nachweise

ORD-Eintrag
ord-f29bb7a1487d41148457acff8bdf0258
Quelldatensatz
uspto-grants-1981_04
Patentnummer
US04263309

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