HomeMCPWorkbenchSkills
HomeWorkbenchNotificationsMe
llms.txt · MCP GuidePrivacy Policy · Terms of Service · Supportv1.8.0
  1. Home
  2. /Reaction

Potassium Hydroxide → (1R,2S)-2-methoxycarbonylcyclopropane-1-carboxylic acid

HRID 498114
Notes
Print preview

Reaction equation

HRID 498114 reaction equation
[C@@H:1]1([C:8]([O:10]C)=[O:9])[CH2:3][C@@H:2]1[C:4]([O:6][CH3:7])=[O:5].[OH-].[K+]>CO>[CH3:7][O:6][C:4]([C@H:2]1[CH2:3][C@H:1]1[C:8]([OH:10])=[O:9])=[O:5]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 14797Potassium HydroxideHCID 642979Dimethyl (1R,2S)-cyclopropane-1,2-dicarboxylate

Product 1

HCID 12510973(1R,2S)-2-methoxycarbonylcyclopropane-1-carboxylic acidYield 92.6%

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

To 150 ml of a methanol solution of 14.68 g (92.8 mmol) of dimethyl cis-1,2-cyclopropanedicarboxylate was added 67 ml of an aqueous solution of 7.52 g (113.9 mmol) of potassium hydroxide under cooling with ice, and the mixture was stirred at room temperature for 24 hours. After completion of the reaction, the solvent was removed by evaporation under reduced pressure, and to the residue was added water. The reaction mixture was washed with diethyl ether. The aqueous layer was adjusted to pH 2 with concentrated hydrochloric acid and extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure to give 12.38 g (92.5%) of the title compound as a colorless oily substance.

Workup

  1. temperatureunder cooling with ice
  2. customAfter completion of the reaction
  3. customthe solvent was removed by evaporation under reduced pressure
  4. additionto the residue was added water
  5. washThe reaction mixture was washed with diethyl ether
  6. extractionextracted with ethyl acetate
  7. dry with materialThe organic layer was dried over anhydrous sodium sulfate
  8. customthe solvent was evaporated under reduced pressure

Sources & evidence

ORD record
ord-f8ca7fa0ed9a412fae5f876e19778033
Source dataset
uspto-grants-2005_09
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06949662B2

Reaction notes

Loading…

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes