Water → 2-(2-Decylindan-5-yl)-5-(3-phenylpropyloxy)pyrimidine

HRID 2211073Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2211073
[CH2:1]([CH:11]1[CH2:19][C:18]2[C:13](=[CH:14][CH:15]=[C:16]([C:20]3[N:25]=[CH:24][C:23]([OH:26])=[CH:22][N:21]=3)[CH:17]=2)[CH2:12]1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH3:10].C1(C)C=CC(S(O[CH2:37][CH2:38][CH2:39][C:40]2[CH:45]=[CH:44][CH:43]=[CH:42][CH:41]=2)(=O)=O)=CC=1.[OH-].[K+].O>C(O)C>[CH2:1]([CH:11]1[CH2:19][C:18]2[C:13](=[CH:14][CH:15]=[C:16]([C:20]3[N:25]=[CH:24][C:23]([O:26][CH2:37][CH2:38][CH2:39][C:40]4[CH:45]=[CH:44][CH:43]=[CH:42][CH:41]=4)=[CH:22][N:21]=3)[CH:17]=2)[CH2:12]1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH3:10]

Komponenten

6

Versuchsvorschrift

0.443 g of 2-(2-decylindan-5-yl)pyrimidine-5-ol, 0.343 g of phenylpropyl p-toluenesulfonate and 0.1 g of potassium hydroxide were dissolved in 2 ml of ethanol, followed by heat-refluxing for 4 hours. After the reaction, the reaction mixture was poured into water and subjected to extraction with toluene. The resultant organic layer was washed with water and dried with anhydrous sodium sulfate, followed by distilling-off of the solvent and purification by silica gel column chromatography to obtain 0.313 g of an objective product (Yield: 53.2%).

Aufarbeitung

  1. temperatureby heat-refluxing for 4 hours
  2. customAfter the reaction
  3. extractionsubjected to extraction with toluene
  4. washThe resultant organic layer was washed with water
  5. dry with materialdried with anhydrous sodium sulfate
  6. distillationfollowed by distilling-off of the solvent and purification by silica gel column chromatography

Quellen und Nachweise

ORD-Eintrag
ord-7a8d88ac4e4845b1bd644afc12d679ed
Quelldatensatz
uspto-grants-1995_10
Patentnummer
US05462694

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