Acetic Acid → HCID 21320544, compound
Reaction equation
[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[CH:13]=[CH:12][C:11]([CH:14]([CH3:18])[C:15]([OH:17])=[O:16])=[CH:10][C:9]=2[O:19]C)=[CH:4][CH:3]=1.C(O)(=O)C>Br>[F:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]2[CH:13]=[CH:12][C:11]([CH:14]([CH3:18])[C:15]([OH:17])=[O:16])=[CH:10][C:9]=2[OH:19])=[CH:6][CH:7]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 2-(4'-fluoro-2-methoxy-4-biphenylyl)propionic acid (10 g.) in a mixture of hydrobromic acid (270 ml. of 48% w/v aqueous acid) and glacial acetic acid (90 ml.) was refluxed for 3.5 hours. The resulting solution was poured onto crushed ice, causing the precipitation of a solid product. This product was collected by filtration, washed with water, dried and recrystallised from chloroform/light petroleum (b.p. 62°-68° C.) to give 2-(4'-fluoro-2-hydroxy-4-biphenylyl)propionic acid, m.p. 138°-142° C.
Workup
- temperaturewas refluxed for 3.5 hours
- additionThe resulting solution was poured
- customonto crushed ice
- customthe precipitation of a solid product
- filtrationThis product was collected by filtration
- washwashed with water
- customdried
- customrecrystallised from chloroform/light petroleum (b.p. 62°-68° C.)
Sources & evidence
- ORD record
- ord-eae4ade79c7b47f9ad743b862d097344
- Source dataset
- uspto-grants-1979_05
- Patent number
- US04153807
Reaction notes
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