Water → 1-Trityl-1H-1,2,4-triazole

HRID 11231

Reaktionsgleichung

Reaktionsgleichung von HRID 11231
[H-].[Na+].[NH:3]1[CH:7]=[N:6][CH:5]=[N:4]1.[C:8](Cl)([C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1)([C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1.O>CCCCCC.CN(C=O)C>[C:8]([N:3]1[CH:7]=[N:6][CH:5]=[N:4]1)([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)([C:21]1[CH:22]=[CH:23][CH:24]=[CH:25][CH:26]=1)[C:15]1[CH:16]=[CH:17][CH:18]=[CH:19][CH:20]=1

Komponenten

7

Versuchsvorschrift

Sodium hydride (60% dispersion in mineral oil, 13.8 g, 345 mmol) was washed with hexane and suspended in DMF (150 ml). At an ice bath temperature, 1,2,4-triazole (total; 20.7 g, 300 mmol) was added thereto in four divisions. After stirring for 30 minutes, to the mixture was added tritylchloride (total; 83.7 g, 300 mmol) in seven divisions and additionally added DMF (50 ml). After stirring for 1.5 hours at room temperature, to the reaction mixture was added water (600 ml). The precipitated crystal was collected by filteration, washed with water, dissolved in CHCl3 (800 ml) and dried. The solvent was evaporated. The obtained residue was chromatographed on silica gel (ethylacetate:CHCl3=1:2, v/v). The fraction of the objective was concentrated to give 1-trityl-1H-1,2,4-triazole (43.9 g). Yield: 47%.

Aufarbeitung

  1. stirringAfter stirring for 1.5 hours at room temperature, to the reaction mixture
  2. customThe precipitated crystal was collected by filteration
  3. washwashed with water
  4. dissolutiondissolved in CHCl3 (800 ml)
  5. customdried
  6. customThe solvent was evaporated
  7. customThe obtained residue was chromatographed on silica gel (ethylacetate
  8. concentrationThe fraction of the objective was concentrated

Quellen und Nachweise

ORD-Eintrag
ord-7128cd1309b044118228bc991451e2cd
Quelldatensatz
uspto-grants-2006_08
Patentnummer
US07098201B2

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