Succinic anhydride → HCID 14234801, Verbindung

HRID 974417

Reaktionsgleichung

Reaktionsgleichung von HRID 974417
[CH3:1][C:2]1([CH3:14])[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[C:4]([CH3:12])([CH3:11])[CH:3]1[CH3:13].[C:15]1(=[O:21])[O:20][C:18](=[O:19])[CH2:17][CH2:16]1.[Cl-].[Al+3].[Cl-].[Cl-]>ClCCCl>[CH3:11][C:4]1([CH3:12])[C:5]2[C:10](=[CH:9][C:8]([C:15](=[O:21])[CH2:16][CH2:17][C:18]([OH:20])=[O:19])=[CH:7][CH:6]=2)[C:2]([CH3:14])([CH3:1])[CH:3]1[CH3:13]

Komponenten

5

Versuchsvorschrift

To a solution of 11 g of 1,1,2,3,3-pentamethyl indane (0.058 mole) and 7 g of succinic anhydride (0.07 mole) in 100 cm3 of anhydrous 1,2-dichloroethane, stirred at 0° C., there are added, by small portions, 9.4 g of aluminum chloride in a manner such that the temperature remains lower than 30° C. The reaction mixture is stirred for 3 hours at ambient temperature and then poured into 250 cm3 of ice water. The organic phase is decanted and the aqueous phase is extracted twice with 1,2-dichloroethane. The organic phases are combined, washed with water and dried on magnesium sulfate. The solvent is evaporated under reduced pressure and the resulting product is crystallized in isopropyl ether. 7 g of 4-(1,1,2,3,3-pentamethyl-5-indanyl)-4-oxo butyric acid in the form of white crystals whose melting point is 161° C. are obtained.

Aufarbeitung

  1. customremains lower than 30° C
  2. customThe organic phase is decanted
  3. extractionthe aqueous phase is extracted twice with 1,2-dichloroethane
  4. washwashed with water
  5. customdried on magnesium sulfate
  6. customThe solvent is evaporated under reduced pressure
  7. customthe resulting product is crystallized in isopropyl ether

Quellen und Nachweise

ORD-Eintrag
ord-5baef1fd4be94fc5b57312edb2d45dca
Quelldatensatz
uspto-grants-1991_11
Patentnummer
US05068393

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