Lithium Hydroxide → (2E)-2-(3-chloro-4-methylsulfonylphenyl)-2-propan-2-yloxyiminoacetic acid
Reaction equation
C[O:2][C:3](=[O:21])/[C:4](/[C:10]1[CH:15]=[CH:14][C:13]([S:16]([CH3:19])(=[O:18])=[O:17])=[C:12]([Cl:20])[CH:11]=1)=[N:5]/[O:6][CH:7]([CH3:9])[CH3:8].[OH-].[Li+]>CO.C(Cl)(Cl)Cl>[Cl:20][C:12]1[CH:11]=[C:10](/[C:4](=[N:5]\[O:6][CH:7]([CH3:9])[CH3:8])/[C:3]([OH:21])=[O:2])[CH:15]=[CH:14][C:13]=1[S:16]([CH3:19])(=[O:18])=[O:17]Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Conditions
- Temperature
- 0 °C
Procedure
This estimated 80% pure (E)-(3-chloro-4-methanesulfonyl-phenyl)-isopropoxyimino-acetic acid methyl ester (0.52 g, <1.5 mmol) was dissolved in methanol (14 mL) and cooled to 0° C. An aqueous solution of lithium hydroxide (2.0 N, 1.86 mL, 3.72 mmol) was added dropwise. After stirring 1.25 h, the reaction mixture was diluted with chloroform (175 mL) and washed with 0.2 M aqueous potassium bisulfate solution (50 mL). The aqueous phase was extracted with chloroform (75 mL) and the combined organic phases were dried over magnesium sulfate and evaporated in vacuo to afford (E)-(3-chloro-4-methanesulfonyl-phenyl)-isopropoxyimino-acetic acid (506 mg, quant.) as a slightly yellow paste that was used without further purification.
Workup
- washwashed with 0.2 M aqueous potassium bisulfate solution (50 mL)
- extractionThe aqueous phase was extracted with chloroform (75 mL)
- dry with materialthe combined organic phases were dried over magnesium sulfate
- customevaporated in vacuo
Sources & evidence
- ORD record
- ord-d7ab8075e66745cf9aa6bf14c8bfe38f
- Source dataset
- uspto-grants-2011_03
- Patent number
- US07902248B2
Reaction notes
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