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

HRID 35140

反応式

HRID 35140 の反応式
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

参加物

5

実験手順

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 solvent was heated at 160°-65° 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 l) 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 gel. 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°-65° C. (0.1 mm Hg) to provide the analytical sample.

後処理

  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 gel
  8. washElution with 1:1 hexane

出典と根拠

ORDレコード
ord-002d4db931ae41a19e700f3940ccddd4
出典データセット
uspto-grants-1988_08
特許番号
US04764616

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