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Hydrochloric Acid → Methyl 2-(4-(2-oxopropyl)phenoxy)acetate

HRID 1758985
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1758985
S(S([O-])=O)([O-])(=O)=[O:2].[Na+].[Na+].[C:10]([CH2:14][O:15][C:16]1[CH:21]=[CH:20][C:19]([CH2:22][C:23](=NO)[CH3:24])=[CH:18][CH:17]=1)([O:12][CH3:13])=[O:11].Cl>O.CO>[C:10]([CH2:14][O:15][C:16]1[CH:21]=[CH:20][C:19]([CH2:22][C:23](=[O:2])[CH3:24])=[CH:18][CH:17]=1)([O:12][CH3:13])=[O:11]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 3

HCID 313Hydrochloric AcidHCID 656671Sodium PyrosulfiteHCID 867384661-(4-Carbomethoxymethoxyphenyl)propan-2-one oxime

Produkt 1

HCID 13851156Methyl 2-(4-(2-oxopropyl)phenoxy)acetate

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 887MethanolLösungsmittelHCID 962
Water
Lösungsmittel

Versuchsvorschrift

Sodium metabisulphite (26 g) in water (60 ml) was added to 1-(4-carbomethoxymethoxyphenyl)propan-2-one oxime (7.5 g) in methanol (50 ml) and the mixture refluxed for 6 hours. The reaction mixture was cooled, concentrated hydrochloric acid (30 ml) added and the mixture extracted with ethyl acetate. The combined ethyl acetate extracts were washed with water followed by sodium bicarbonate solution. The ethyl acetate layer was dried (MgSO4) and evaporated to give the title compound as an oil which crystallised on standing, (mp 63°-70°l ). τ (CDCl3) 7.91 (3H, s), 6.30 (2H, s), 6.26 (3H, s), 5.42 (2H, s), 3.17 (2H, d, J=8 Hz), 2.87 (2H, d, J=8 Hz).

Aufarbeitung

  1. temperaturethe mixture refluxed for 6 hours
  2. temperatureThe reaction mixture was cooled
  3. extractionthe mixture extracted with ethyl acetate
  4. washThe combined ethyl acetate extracts were washed with water
  5. dry with materialThe ethyl acetate layer was dried (MgSO4)
  6. customevaporated

Quellen und Nachweise

ORD-Eintrag
ord-79ef9a6af00d412fb24e917f96ff718c
Quelldatensatz
uspto-grants-1982_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04338333

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