Acetic Acid → HCID 20063336, Verbindung

HRID 1084454Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1084454
C([O:3][C:4]([C:6]1(C(OCC)=O)[C:16](O)([CH:17]([CH3:19])[CH3:18])[C:15]2[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=2)[C:8](=[O:9])[O:7]1)=[O:5])C.C(O)(=O)C.Cl.C(=O)([O-])O.[Na+]>O>[CH:17]([C:16]1[C:15]2[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=2)[C:8](=[O:9])[O:7][C:6]=1[C:4]([OH:5])=[O:3])([CH3:19])[CH3:18]

Komponenten

6

Versuchsvorschrift

A stirred mixture of crude 3,3-bis(ethoxycarbonyl)-4-hydroxy-4-isopropyl-3,4-dihydroisocoumarin (76 g), glacial acetic acid (500 ml) and concentrated hydrochloric acid (800 ml) was refluxed for 18 hours. The cooled mixture was added to ice/water (3500 ml) and the precipitated solid filtered off and washed with water to give an off-white solid. This was treated with a solution of sodium hydrogen carbonate (40 g) in water (400 ml) and the resultant solution was extracted with diethyl ether (150 ml). The aqueous phase was acidified to pH1 with concentrated hydrochloric acid and the white precipitate filtered off, washed with water and dried at 70° C. to give 4-isopropylisocoumarin-3-carboxylic acid (20.16 g) in the form of a white solid [Elemental analysis: C, 67.4; H, 5.2%; calculated: C, 67.2; H, 5.17%; NMR (in DMSO-d6): 1.45 (6H, d, J=8 Hz), 3.85 (1H, sept, J=8 Hz), 7.6-8.4 (4H, m)].

Aufarbeitung

  1. temperaturewas refluxed for 18 hours
  2. filtrationthe precipitated solid filtered off
  3. washwashed with water
  4. customto give an off-white solid
  5. extractionthe resultant solution was extracted with diethyl ether (150 ml)
  6. filtrationthe white precipitate filtered off
  7. washwashed with water
  8. customdried at 70° C.

Quellen und Nachweise

ORD-Eintrag
ord-7ecfebc3723645c8a8d71f83e2d8acdb
Quelldatensatz
uspto-grants-1991_04
Patentnummer
US05004747

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