Water → 2-(4-Chlorophenyl)cyclopropanecarboxylic acid
Reaction equation
CON(C)[C:4]([CH:6]1[CH2:8][CH:7]1[C:9]1[CH:14]=[CH:13][C:12]([Cl:15])=[CH:11][CH:10]=1)=[O:5].[OH2:17].[OH-].[Na+]>CO>[Cl:15][C:12]1[CH:13]=[CH:14][C:9]([CH:7]2[CH2:8][CH:6]2[C:4]([OH:17])=[O:5])=[CH:10][CH:11]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 2-(4-chloro-phenyl)-cyclopropanecarboxylic acid methoxy-methyl-amide (9.6 g), water (20 mL), and NaOH (3.2 g) in MeOH (40 mL) was refluxed for 3 h. The reaction mixture was cooled down to room temperature and concentrated in vacuo. The residue was acidified by 6 N HCl followed by extraction with CH2Cl2. The organic layer was washed with brine, dried over MgSO4 and concentrated in vacuo to give the title compound (7.3 g).
Workup
- temperaturewas refluxed for 3 h
- concentrationconcentrated in vacuo
- extractionfollowed by extraction with CH2Cl2
- washThe organic layer was washed with brine
- dry with materialdried over MgSO4
- concentrationconcentrated in vacuo
Sources & evidence
- ORD record
- ord-0c3548e2bf0040538a7899810ba057d3
- Source dataset
- uspto-grants-2006_12
- Patent number
- US07144881B2
Reaction notes
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