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

HRID 653957

Reaction equation

HRID 653957 reaction equation
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

Participants

5

Conditions

Temperature
25 °C

Procedure

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.

Workup

  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

Sources & evidence

ORD record
ord-4564e893faf94e44992f541553deceb4
Source dataset
uspto-grants-1992_07
Patent number
US05128448

Linked notes

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