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Sodium Acetate → 2-Methoxycarbonyl-3-chloro4-(acetoxymethyl)thiophene

HRID 2300915
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2300915
[CH3:1][O:2][C:3]([C:5]1[S:6][CH:7]=[C:8]([CH2:11]Cl)[C:9]=1[Cl:10])=[O:4].[C:13]([O-:16])(=[O:15])[CH3:14].[Na+]>C(O)(=O)C>[CH3:1][O:2][C:3]([C:5]1[S:6][CH:7]=[C:8]([CH2:11][O:16][C:13](=[O:15])[CH3:14])[C:9]=1[Cl:10])=[O:4]
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Komponenten

4

Edukt 2

HCID 517045Sodium AcetateHCID 183767792-Methoxycarbonyl-3-chloro4-(chloromethyl)thiophene

Produkt 1

HCID 183769232-Methoxycarbonyl-3-chloro4-(acetoxymethyl)thiopheneAusbeute 90 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 176Acetic AcidLösungsmittel

Versuchsvorschrift

To 2-methoxycarbonyl-3-chloro4-(chloromethyl)thiophene (48 g, 0.21 mol) in glacial acetic acid (500 mL) was added sodium acetate (35 g, 0.42 mol). The reaction was heated at reflux for 24 hours, then cooled and concentrated in vacuo. The residual oil was made basic by addition of saturated aqueous sodium bicarbonate, and the resulting solution extracted with ethyl acetate (4×150 mL). The combined extracts were dried over sodium sulfate and concentrated to afford 47 g (90% yield) of 2-methoxycarbonyl-3-chloro4-(acetoxymethyl)thiophene as, a light brown oil; NMR (CDCl3) 7.6 (s, 1), 5.1 (s, 2), 3.9 (s, 3), 2.1 (s, 3) ppm.

Aufarbeitung

  1. temperatureThe reaction was heated
  2. temperatureat reflux for 24 hours
  3. temperaturecooled
  4. concentrationconcentrated in vacuo
  5. additionThe residual oil was made basic by addition of saturated aqueous sodium bicarbonate
  6. extractionthe resulting solution extracted with ethyl acetate (4×150 mL)
  7. dry with materialThe combined extracts were dried over sodium sulfate
  8. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-254486f29ba24900afc192da078fc742
Quelldatensatz
uspto-grants-2002_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06498185B1

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