Water → Benzo[b]thiophene-2-propionic acid

HRID 653957

Reaktionsgleichung

Reaktionsgleichung von HRID 653957
C([O:3][C:4](=[O:16])[CH2:5][CH2:6][C:7]1[S:11][C:10]2[CH:12]=[CH:13][CH:14]=[CH:15][C:9]=2[CH:8]=1)C.[OH-].[K+].CO.O>CO>[S:11]1[C:7]([CH2:6][CH2:5][C:4]([OH:16])=[O:3])=[CH:8][C:9]2[CH:15]=[CH:14][CH:13]=[CH:12][C:10]1=2

Komponenten

5

Reaktionsbedingungen

Temperatur
25 °C

Versuchsvorschrift

To a solution of benzo[b]thiophene-2-propanoic acid ethyl ester (3.52 g, 15.0 mmol) in MeOH (200 mL) was added at 0° C. 10% KOH/MeOH (70 mL, 144 mmol) and H2O (30 mL). The solution was stirred at 25° C. for 6 h then kept in a refrigerator (0° C.) overnight. After addition of H2O (20 mL), the mixture was concentrated under reduced pressure to remove most of MeOH then acidified carefully with 3N HCl to pH 2. The resultant turbid mixture was extracted with Et2O (3×500 mL). The combined extracts were washed with brine (200 mL), dried (MgSO4), and concentrated to dryness to give benzo[b]thiophene-2-propanoic acid (3.04 g, 14.7 mmol) in 98% yield as a solid, mp 140°-142° C.

Aufarbeitung

  1. customthen kept in a refrigerator (0° C.) overnight
  2. concentrationthe mixture was concentrated under reduced pressure
  3. customto remove most of MeOH
  4. extractionThe resultant turbid mixture was extracted with Et2O (3×500 mL)
  5. washThe combined extracts were washed with brine (200 mL)
  6. dry with materialdried (MgSO4)
  7. concentrationconcentrated to dryness

Quellen und Nachweise

ORD-Eintrag
ord-4564e893faf94e44992f541553deceb4
Quelldatensatz
uspto-grants-1992_07
Patentnummer
US05128448

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