Sodium Hydroxide → (2-tert-butylphenyl)(1H-imidazol-2-yl)phenylmethanol

HRID 261953노트

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HRID 261953 반응식
[C:1]([C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][C:6]=1[C:11]([C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1)([C:13]1[N:14](C=C)[CH:15]=[CH:16][N:17]=1)[OH:12])([CH3:4])([CH3:3])[CH3:2].[OH-].[Na+].[Mn]([O-])(=O)(=O)=O.[K+].[Mn]([O-])(=O)(=O)=O>N1C=CC=CC=1>[C:1]([C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][C:6]=1[C:11]([C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1)([C:13]1[NH:14][CH:15]=[CH:16][N:17]=1)[OH:12])([CH3:4])([CH3:2])[CH3:3]

참가 물질

6

실험 절차

To a solution of 10.0 g. (0.03 mol) of α-(o-tert.-butylphenyl)-α-phenyl-1-vinylimidazole-2-methanol in 180 ml. of pyridine and 180 ml. of 0.5 N methanolic sodium hydroxide, 360 ml. of a 4% aqueous potassium permanganate solution were added drop-wise at 20° to 30° C. After the addition was completed, 4.8 g. of solid potassium permanganate were added (total permanganate 0.12 mol). The manganese dioxide was filtered off. The filtrate was treated with active charcoal, concentrated almost to complete dryness and poured into water. The solid substance was filtered off, dissolved in warm acetone, decolorised with active charcoal and precipitated by addition of water. The precipitate was recrystallised from a mixture of acetone and water. α-(o-tert.-Butylphenyl)-α-phenylimidazole-2-methanol was obtained. Melting point 185°-186° C.

후처리

  1. additionAfter the addition
  2. filtrationThe manganese dioxide was filtered off
  3. additionThe filtrate was treated with active charcoal
  4. concentrationconcentrated almost to complete dryness
  5. additionpoured into water
  6. filtrationThe solid substance was filtered off
  7. dissolutiondissolved in warm acetone
  8. customprecipitated by addition of water
  9. customThe precipitate was recrystallised from a mixture of acetone and water

출처 및 근거

ORD 기록
ord-6e33305add3a48208c16a1a02deff329
출처 데이터셋
uspto-grants-1979_05
특허 번호
US04152441

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