Water → HCID 21187833, compound

HRID 1383548Notes

Reaction equation

HRID 1383548 reaction equation
C(=O)([O-])[O-].[K+].[K+].O.[CH:8]1([O:13][C:14]2[CH:15]=[C:16]([CH:21]=[CH:22][C:23]=2[O:24][C:25]([F:28])([F:27])[F:26])[C:17]([O:19]C)=[O:18])[CH2:12][CH2:11][CH2:10][CH2:9]1>CO>[CH:8]1([O:13][C:14]2[CH:15]=[C:16]([CH:21]=[CH:22][C:23]=2[O:24][C:25]([F:26])([F:27])[F:28])[C:17]([OH:19])=[O:18])[CH2:9][CH2:10][CH2:11][CH2:12]1

Participants

5

Procedure

Potassium carbonate (0.43 g) and water (2 mL) are added to a solution of methyl 3-cyclopentyloxy-4-trifluoromethoxybenzoate (0.78 g) in methanol (10 mL) and the mixture is heated under reflux for 2 hours. Methanol is evaporated off under reduced pressure, and the crude material is partitioned between water (75 mL) and ethyl acetate (75 mL). The organic layer is separated, and the aqueous layer is acidified with hydrochloric acid (2 N) and extracted with ethyl acetate (2×75 mL). The combined organic extracts are dried over magnesium sulfate and evaporated under reduced pressure, to give 3-cyclopentyloxy-4-trifluoromethoxybenzoic acid (0.53 g), in the form of a white solid, m.p. 116-118° C. [NMR (CDCl3): 7.72(d,1H,J=2 Hz); 7.7(dd,1H,J=8 Hz, 2 Hz); 7.3(d,1H,J=8 Hz); 4.9(m,1H,);2.0-1.6(m,8H)].

Workup

  1. temperaturethe mixture is heated
  2. temperatureunder reflux for 2 hours
  3. customMethanol is evaporated off under reduced pressure
  4. customthe crude material is partitioned between water (75 mL) and ethyl acetate (75 mL)
  5. customThe organic layer is separated
  6. extractionextracted with ethyl acetate (2×75 mL)
  7. dry with materialThe combined organic extracts are dried over magnesium sulfate
  8. customevaporated under reduced pressure

Sources & evidence

ORD record
ord-b98fb4fef9064d25b743952a2c2db591
Source dataset
uspto-grants-2001_07
Patent number
US06255326B1

Reaction notes

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