Hydrochloric Acid → 2-p-Ethoxyphenyl acrylic acid
Reaction equation
C([O:3][C:4](=[O:17])[CH:5]([C:8]1[CH:13]=[CH:12][C:11]([O:14][CH2:15][CH3:16])=[CH:10][CH:9]=1)[CH2:6]O)C.Cl>[OH-].[K+]>[CH2:15]([O:14][C:11]1[CH:12]=[CH:13][C:8]([C:5](=[CH2:6])[C:4]([OH:17])=[O:3])=[CH:9][CH:10]=1)[CH3:16]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The ethyl-2-p-ethoxyphenyl-3-hydroxypropionate (0.7 g) was refluxed for 7 h in potassium hydroxide solution (20%, 2 ml). It was acidified with dilute HCl and the crude acid (0.46 g, m.p. 103°-107°) used for the next step without further purification.
Workup
- customthe crude acid (0.46 g, m.p. 103°-107°) used for the next step without further purification
Sources & evidence
- ORD record
- ord-e97a6da48f7749f1a46ed8a5ec1265c5
- Source dataset
- uspto-grants-1982_01
- Patent number
- US04309350
Reaction notes
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