Hydrochloric Acid → HCID 15572235, compound
Reaction equation
[CH3:1][C:2]1[CH:7]=[C:6]([C:8]([OH:17])([C:13]([F:16])([F:15])[F:14])[C:9]([F:12])([F:11])[F:10])[CH:5]=[C:4]([CH3:18])[C:3]=1[NH:19][CH2:20][C:21]([O:23]CC)=[O:22].Cl>[OH-].[Na+]>[C:21]([CH2:20][NH:19][C:3]1[C:2]([CH3:1])=[CH:7][C:6]([C:8]([OH:17])([C:13]([F:15])([F:14])[F:16])[C:9]([F:10])([F:11])[F:12])=[CH:5][C:4]=1[CH3:18])([OH:23])=[O:22]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Dissolve ethyl N-[2,6-dimethyl-4-(hexafluoro-2-hydroxy-2-propyl)phenyl]glycinate (3.1 g, 8.3 mmol) in 25 ml 1.0 N NaOH. After 1 hour, add 25 ml 1.0 N HCl and extract with ethyl acetate. Dry and concentrate. Recrystallize from chloroform-benzene to give the title compound as beige solid, m.p. 153°-155° C. dec.
Workup
- extractionextract with ethyl acetate
- customDry
- concentrationconcentrate
- customRecrystallize from chloroform-benzene
Sources & evidence
- ORD record
- ord-cf6f348677f34fa2a6fb539f05d7caf0
- Source dataset
- uspto-grants-1981_05
- Patent number
- US04267193
Reaction notes
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