2,4,6-Trimethylpyridine → 1-(4-Bromo-2-nitrophenyl)-1,2,3,4-tetrahydroquinoline

HRID 34390

Reaktionsgleichung

Reaktionsgleichung von HRID 34390
Br[C:2]1[CH:7]=[CH:6][C:5]([Br:8])=[CH:4][C:3]=1[N+:9]([O-:11])=[O:10].[NH:12]1[C:21]2[C:16](=[CH:17][CH:18]=[CH:19][CH:20]=2)[CH2:15][CH2:14][CH2:13]1.N1C(C)=CC(C)=CC=1C>CC1C=CC=C(C)C=1C>[Br:8][C:5]1[CH:6]=[CH:7][C:2]([N:12]2[C:21]3[C:16](=[CH:17][CH:18]=[CH:19][CH:20]=3)[CH2:15][CH2:14][CH2:13]2)=[C:3]([N+:9]([O-:11])=[O:10])[CH:4]=1

Komponenten

5

Edukt 3

HCID 79532,4,6-TrimethylpyridineHCID 694601,2,3,4-TetrahydroquinolineHCID 770041,4-Dibromo-2-nitrobenzene

Produkt 1

HCID 138129271-(4-Bromo-2-nitrophenyl)-1,2,3,4-tetrahydroquinolineAusbeute 18 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 106861,2,3-TrimethylbenzeneLösungsmittel

Versuchsvorschrift

A stirred mixture, under nitrogen, of 2,5-dibromonitrobenzene (140.5 g, 0.50 mole), 1,2,3,4-tetrahydroquinoline (133.2 g, 1.00 mole) and symmetrical collidine (121.2 g 1.00 mole) in 1,2,3-trimethylbenzene (500 ml) as solvents was heated at 160°-165° C. for 7 days. The mixture was cooled to room temperature, filtered, and the filtrate was concentrated in vacuo (100° C.). The residue was taken up in dichloromethane (1.5 1) and the solution was extracted three times with dilute hydrochloric acid, once with dilute sodium hydroxide solution, three times with water, dried over anhydrous sodium sulfate and concentrated. This residue was dissolved in 1:1 hexane:toluene (250 ml) and adsorbed on a chromatography column containing 3 kg of silica el. Elution with 1:1 hexane:toluene gave 30 g (18%) of product, as an oil. A portion of the oil was Kugelrohr distilled at an oven-temperature of 163°-165° C. (0.1 mm Hg) to provide the analytical sample.

Aufarbeitung

  1. filtrationfiltered
  2. concentrationthe filtrate was concentrated in vacuo (100° C.)
  3. extractionthe solution was extracted three times with dilute hydrochloric acid
  4. dry with materialonce with dilute sodium hydroxide solution, three times with water, dried over anhydrous sodium sulfate
  5. concentrationconcentrated
  6. dissolutionThis residue was dissolved in 1:1 hexane
  7. additioncontaining 3 kg of silica el
  8. washElution with 1:1 hexane

Quellen und Nachweise

ORD-Eintrag
ord-1e47a9ff0f4d46808118082466f52e38
Quelldatensatz
uspto-grants-1988_08
Patentnummer
US04761412

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