Sodium Hydroxide → HCID 19359190, compound
Reaction equation
C([O:3][C:4](=[O:17])[CH:5]([C:8]1[CH:13]=[CH:12][C:11]([C:14](=[O:16])[CH3:15])=[CH:10][CH:9]=1)[CH2:6][CH3:7])C.[OH-].[Na+]>C(O)C.O>[C:14]([C:11]1[CH:12]=[CH:13][C:8]([CH:5]([CH2:6][CH3:7])[C:4]([OH:17])=[O:3])=[CH:9][CH:10]=1)(=[O:16])[CH3:15]Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
Part C--To a solution of 4-acetylphenylbutyric acid ethyl ester (50.0 g, 0.21 mol) in ethanol (1250 mL) was added, dropwise, a solution of sodium hydroxide (50.0 g) in water (1250 mL). All was stirred at reflux over 4 hours. The solution was concentrated to half volume and then acidified to a pH equal to 1.0 using hydrochloric acid (1N). The resulting precipitate was collected and washed with water to give 4-acetylphenylbutyric acid (53.76 g, 0.26 mol, 99%) as a white solid. mp=50°-52° C.;
Workup
- temperatureat reflux over 4 hours
- concentrationThe solution was concentrated to half volume
- customThe resulting precipitate was collected
- washwashed with water
Sources & evidence
- ORD record
- ord-506a29a7e25540f4b7d412187d50ce42
- Source dataset
- uspto-grants-1997_06
- Patent number
- US05635477
Reaction notes
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