Acetic Anhydride → 1,3-Cyclopentanedicarboxylic anhydride

HRID 1253257

Reaktionsgleichung

Reaktionsgleichung von HRID 1253257
[CH:1]1([C:9]([OH:11])=[O:10])[CH2:5][CH2:4][CH:3]([C:6]([OH:8])=O)[CH2:2]1.C(OC(=O)C)(=O)C>>[CH:3]12[C:6](=[O:8])[O:11][C:9](=[O:10])[CH:1]([CH2:5][CH2:4]1)[CH2:2]2

Komponenten

3

Edukt 2

HCID 7918Acetic AnhydrideHCID 1072161,3-Cyclopentanedicarboxylic acid

Produkt 1

HCID 2397991,3-Cyclopentanedicarboxylic anhydride

Versuchsvorschrift

1,3-Cyclopentanedicarboxylic acid (4.0 g., 25 mmole) was converted to the anhydride by refluxing for 3 hours in 20 ml. of acetic anhydride. After removal of excess acetic anhydride, extraction with hexane and evaporation of the hexane, 3.95 g. of cyclopentane-1,3-dicarboxylic anhydride was obtained. The anhydride was combined with 6.51 g. (27 mmole) of 1-(4-aminobutyl)-4-(2-pyrimidinyl)piperazine in 50 ml. of dichloromethane and stirred at room temperature overnight. The dichloromethane was removed in vacuo and replaced with 75 ml. of toluene. The mixture was refluxed for 24 hours with water separation via a Dean-Stark trap. The product was concentrated under vacuum and chromatographed on 200 g. of silica gel with 5% ethanol/chloroform. The product-containing fractions were combined and concentrated and the residue crystallized (2 crops) from isopropanol with addition of 4N HCl/isopropanol. A second recrystallization from isopropanol gave 1.1 g. of the title compound as the dihydrochloride, hemihydrate; m.p. 201°-203° C.(d).

Aufarbeitung

  1. temperatureby refluxing for 3 hours in 20 ml
  2. customAfter removal of excess acetic anhydride, extraction
  3. customwith hexane and evaporation of the hexane, 3.95 g

Quellen und Nachweise

ORD-Eintrag
ord-20b008dc52f5489cb975df2baeb20d85
Quelldatensatz
uspto-grants-1988_05
Patentnummer
US04748240

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