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Potassium Hydroxide → 4-(3-(2,6-Dimethylbenzyloxy)phenyl)4-oxobutyric acid Potassium salt

HRID 1039412
Notes
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Reaction equation

HRID 1039412 reaction equation
[CH3:1][C:2]1[CH:22]=[CH:21][CH:20]=[C:19]([CH3:23])[C:3]=1[CH2:4][O:5][C:6]1[CH:7]=[C:8]([C:12](=[O:18])[CH2:13][CH2:14][C:15]([OH:17])=[O:16])[CH:9]=[CH:10][CH:11]=1.[OH-].[K+:25]>C(O)C>[K+:25].[CH3:23][C:19]1[CH:20]=[CH:21][CH:22]=[C:2]([CH3:1])[C:3]=1[CH2:4][O:5][C:6]1[CH:7]=[C:8]([C:12](=[O:18])[CH2:13][CH2:14][C:15]([O-:17])=[O:16])[CH:9]=[CH:10][CH:11]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 14797Potassium HydroxideHCID 9926783HCID 9926783, compound

Product 1

HCID 208123284-(3-(2,6-Dimethylbenzyloxy)phenyl)4-oxobutyric acid Potassium salt

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

The 4-(3-(2,6-Dimethylbenzyloxy)phenyl)-4-oxobutyric acid (Step D, 6.0 g, 19.4 mmol) was dissolved in abs ethanol (20 ml) by warming gently followed by addition of KOH (1.21 g) at 0° C. temperature. The reaction mixture was stirred for one hour, concentrated in vaccuo and lyophilized to give the title compound as white solid.

Workup

  1. temperatureby warming gently
  2. concentrationconcentrated in vaccuo

Sources & evidence

ORD record
ord-4bcda6a7f669458aa7422439bc10c0a4
Source dataset
uspto-grants-2013_10
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08552062B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes