Water → HCID 22618899, compound

HRID 842287Notes

Reaction equation

HRID 842287 reaction equation
[OH-].[K+].[CH2:3]([C:5]([CH2:16][CH2:17][C:18]1[CH:23]=[CH:22][C:21]([O:24][CH2:25][CH2:26][CH2:27][CH2:28][C:29]2[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=2)=[CH:20][CH:19]=1)([C:11]([O:13]CC)=[O:12])[C:6]([O:8][CH2:9][CH3:10])=[O:7])[CH3:4].O>C(O)C>[CH2:9]([O:8][C:6]([C:5]([CH2:3][CH3:4])([CH2:16][CH2:17][C:18]1[CH:19]=[CH:20][C:21]([O:24][CH2:25][CH2:26][CH2:27][CH2:28][C:29]2[CH:30]=[CH:31][CH:32]=[CH:33][CH:34]=2)=[CH:22][CH:23]=1)[C:11]([OH:13])=[O:12])=[O:7])[CH3:10]

Participants

5

Procedure

Potassium hydroxide (14 g) was added to a solution of diethyl 2-ethyl-2-(2-(4-(4-phenylbutyloxy)phenyl)ethyl)malonate (46 g) in ethanol (300 ml) and the mixture was refluxed under heating for 3.5 hours. The reaction mixture was poured into water and washed with isopropyl ether. After being acidified to pH 1 with concentrated hydrochloric acid, the aqueous layer was extracted with ethyl acetate. The ethyl acetate layer was washed with a saturated brine and dried over anhydrous sodium sulfate, and the solvent was distilled away under reduced pressure to give the subject compound (23 g).

Workup

  1. temperaturethe mixture was refluxed
  2. temperatureunder heating for 3.5 hours
  3. washwashed with isopropyl ether
  4. extractionthe aqueous layer was extracted with ethyl acetate
  5. washThe ethyl acetate layer was washed with a saturated brine
  6. dry with materialdried over anhydrous sodium sulfate
  7. distillationthe solvent was distilled away under reduced pressure

Sources & evidence

ORD record
ord-b8d0b245805d41b8bbcd9cb23133a7d2
Source dataset
uspto-grants-2002_04
Patent number
US06372800B1

Reaction notes

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