(4-Fluoro-3-phenoxyphenyl)methanol → 2,2-Dimethyl-3-(3-cyclopropylmethoxy-3-oxo-1-propenyl) cyclopropane-carboxylic acid
Reaction equation
[CH3:1][C:2]1([CH3:17])[CH:4]([CH:5]=[CH:6][C:7]([O:9][CH2:10][CH:11]2[CH2:13][CH2:12]2)=[O:8])[CH:3]1[C:14]([OH:16])=[O:15].O(C1C=C(CO)C=CC=1F)C1C=CC=CC=1>C(Cl)(Cl)Cl>[CH3:1][C:2]1([CH3:17])[CH:4]([CH:5]=[CH:6][C:7]([O:9][CH2:10][CH:11]2[CH2:13][CH2:12]2)=[O:8])[CH:3]1[C:14]([OH:16])=[O:15].[CH3:1][C:2]1([CH3:17])[CH:4]([CH:5]=[CH:6][C:7]([O:9][CH3:10])=[O:8])[CH:3]1[C:14]([O-:16])=[O:15]Participants
5
Reactant 2
Product 2
Reagents, catalysts & solvents 1
Procedure
Using the procedure of Example 9, (1R, cis, ΔZ) 2,2-dimethyl-3-(3-methoxy-3-oxo-1-propenyl)-cyclopropane-carboxylic acid and (3-phenoxy-4-fluoro-phenyl)-methanol were reacted to obtain (3-phenoxy-4-fluoro-phenyl)-methyl (1R, cis, ΔZ) 2,2-dimethyl-3-(3-methoxy-3-oxo-1-propenyl)-cyclopropane-carboxylate with a specific rotation of [α]D20 =+50.5°±2.5° (c=0.75% in chloroform).
Workup
- customwere reacted
Sources & evidence
- ORD record
- ord-62d5a46c073f49559ad82da46c756fc0
- Source dataset
- uspto-grants-1989_05
- Patent number
- US04833163
Reaction notes
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