Ethanol → HCID 70372312, compound
Reaction equation
[CH3:1]/[C:2](=[CH:8]\[CH2:9][CH2:10][C:11]#[C:12][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)/[C:3]([O:5]CC)=[O:4].C(O)C.[OH-].[K+]>O>[CH3:1]/[C:2](=[CH:8]\[CH2:9][CH2:10][C:11]#[C:12][C:13]1[CH:14]=[CH:15][CH:16]=[CH:17][CH:18]=1)/[C:3]([OH:5])=[O:4]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
The ethyl 2-methyl-7-phenyl-(2E)-heptene-6-ynoate (1.0 g, 4.13 mmol), ethanol (4 ml), potassium hydroxide (1 g) and water (4 ml) were heated together under a nitrogen atmosphere at 50° C. for 2 hours. The reaction mixture was worked up as in Example 1 to give 0.84 g (95% of theory) of 2-methyl-7-phenyl-(2E)-hepten-6-ynoic acid as a colourless solid.
Sources & evidence
- ORD record
- ord-2d949c88833547d2b6178cd21734883d
- Source dataset
- uspto-grants-1990_06
- Patent number
- US04931469
Reaction notes
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