Acetic Acid → HCID 21431786, compound
Reaction equation
[CH:1]1([C:7]([C:9]2[CH:14]=[CH:13][C:12](CC#N)=[CH:11][CH:10]=2)=[O:8])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.S(=O)(=O)(O)O.[C:23]([OH:26])(=[O:25])[CH3:24]>O>[CH:9]1([C:7]([C:1]2[CH:2]=[CH:3][C:4]([CH2:24][C:23]([OH:26])=[O:25])=[CH:5][CH:6]=2)=[O:8])[CH2:10][CH2:11][CH2:12][CH2:13][CH2:14]1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
4-cyclohexylcarbonylphenylacetonitrile (1.5 g.), water (1.5 ml.), concentrated sulphuric acid (1.5 ml.) and acetic acid (1.5 ml.) were heated under reflux for 6 hours, cooled, poured into water and extracted with ether. Removal of the solvent and crystallisation from cyclohexane gave the acid, m.p. 94°-95.5°.
Workup
- temperatureunder reflux for 6 hours
- temperaturecooled
- extractionextracted with ether
- customRemoval of the solvent and crystallisation from cyclohexane
- customgave the acid, m.p. 94°-95.5°
Sources & evidence
- ORD record
- ord-f0bac9bdc3094ef4b917066c8f7467f7
- Source dataset
- uspto-grants-1977_06
- Patent number
- US04028404
Reaction notes
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