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Water → 4-Methoxy-3-isochromanone

HRID 617399
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 617399
C1(C)C=CC(S([O-])(=O)=O)=CC=1.[NH+]1C=CC=CC=1.[CH3:18][O:19][CH:20]([C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][C:27]=1[CH2:32][O:33][CH:34]1CCCC[O:35]1)C(OCC)=O.O>CO>[CH3:18][O:19][CH:20]1[C:26]2[C:27](=[CH:28][CH:29]=[CH:30][CH:31]=2)[CH2:32][O:33][C:34]1=[O:35]
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Komponenten

5

Edukt 3

HCID 962WaterHCID 466102Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 18357803Ethyl alpha-methoxy-2-(tetrahydropyran-2-yloxymethyl)phenylacetate

Produkt 1

HCID 155472854-Methoxy-3-isochromanoneAusbeute 74,2 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 887MethanolLösungsmittel

Versuchsvorschrift

Pyridinium p-toluenesulfonate (0.30 g) was added to a solution of ethyl α-methoxy-2-(tetrahydropyran-2-yloxy-methyl)phenylacetate (14.00 g, 45.4 mmol) in methanol (50 ml), and the mixture was heated under reflux for 1 hour. The mixture was cooled to room temperature, and water (50 ml) was added. The mixture was extracted with methylene chloride and dried over anhydrous magnesium sulfate. The solvent was evaporated, and the residue was purified by recrystallization from n-hexane/ethyl acetate (=1/1) to give the desired compound 4-methoxy-3-isochromanone (6.00 g, 74.2%) as white crystals.

Aufarbeitung

  1. temperaturethe mixture was heated
  2. temperatureunder reflux for 1 hour
  3. extractionThe mixture was extracted with methylene chloride
  4. dry with materialdried over anhydrous magnesium sulfate
  5. customThe solvent was evaporated
  6. customthe residue was purified by recrystallization from n-hexane/ethyl acetate (=1/1)

Quellen und Nachweise

ORD-Eintrag
ord-5f8fd03e8b974d4cb63bfdc7c3fcf2fc
Quelldatensatz
uspto-grants-1999_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05948819

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