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Ethanol → Ethyl 2-[4-(cyclopropanecarbonyl)phenyl]-2-methylpropanoate

HRID 1066485
Notes
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Reaction equation

HRID 1066485 reaction equation
[CH:1]1([C:4]([C:6]2[CH:11]=[CH:10][C:9]([C:12]([CH3:17])([CH3:16])[C:13](N)=[O:14])=[CH:8][CH:7]=2)=[O:5])[CH2:3][CH2:2]1.[CH2:18]([OH:20])[CH3:19]>>[CH:1]1([C:4]([C:6]2[CH:11]=[CH:10][C:9]([C:12]([CH3:17])([CH3:16])[C:13]([O:20][CH2:18][CH3:19])=[O:14])=[CH:8][CH:7]=2)=[O:5])[CH2:3][CH2:2]1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 702EthanolHCID 234998512-(4-Cyclopropanecarbonyl-phenyl)-2-methylpropionamide

Product 1

HCID 9813859Ethyl 2-[4-(cyclopropanecarbonyl)phenyl]-2-methylpropanoate

Procedure

Dissolve 2-(4-cyclopropanecarbonyl-phenyl)-2-methyl-propionamide (100 mg) in ethanol and bubble in hydrochloride gas for 5 minutes while stirring. Reflux for 10 hours, distill off the ethanol and extract into ethyl acetate. Evaporate the solvent in vacuo to give the title compound as an oil (50 mg).

Workup

  1. custombubble in hydrochloride gas for 5 minutes
  2. temperatureReflux for 10 hours
  3. distillationdistill off the ethanol
  4. extractionextract into ethyl acetate
  5. customEvaporate the solvent in vacuo
On this pageParticipantsProcedureWorkupSources & evidenceReaction notes

Sources & evidence

ORD record
ord-209a58a29fce443c86c0660072a0ba45
Source dataset
uspto-grants-2001_06
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06242606B1

Reaction notes

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