Sodium Hydroxide → HCID 23717791, compound
Reaction equation
[CH2:1]([C:6]1[CH:11]=[CH:10][C:9]([CH:12]([CH3:16])[C:13]([OH:15])=[O:14])=[CH:8][CH:7]=1)[CH:2]=[C:3]([CH3:5])[CH3:4].[OH-].[Na+:18]>>[CH2:1]([C:6]1[CH:7]=[CH:8][C:9]([CH:12]([CH3:16])[C:13]([O-:15])=[O:14])=[CH:10][CH:11]=1)[CH:2]=[C:3]([CH3:5])[CH3:4].[Na+:18]Participants
3
Procedure
4.8 g of 2-(p-prenylphenyl)propionic acid as prepared in Example 1 was dissolved in 5% aqueous sodium hydroxide solution to adjust to pH 9.0. After evaporation of the water, the resulting solid was recystallized from ethyl acetate to give 4.5 g of sodium 2-(p-prenylphenyl)propionate, colorless prisms, m.p. 65°-66° C.
Workup
- customAfter evaporation of the water
Sources & evidence
- ORD record
- ord-0ad9b185ceb1465882d6c3bea7e8b5ff
- Source dataset
- uspto-grants-1981_02
- Patent number
- US04251543
Reaction notes
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