Potassium Hydroxide → HCID 59775205, compound
Reaction equation
[F:1][C:2]1[CH:14]=[CH:13][C:5]([O:6][CH2:7][C:8]([O:10]CC)=[O:9])=[CH:4][C:3]=1[CH3:15].[OH-].[K+]>O1CCOCC1>[F:1][C:2]1[CH:14]=[CH:13][C:5]([O:6][CH2:7][C:8]([OH:10])=[O:9])=[CH:4][C:3]=1[CH3:15]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To the solution of ethyl 2-(4-fluoro-3-methylphenoxy)acetate (1.1 g, 5.1 mmol) in 10 mL dioxane was added 10 mL aqueous 5% KOH at 25° C. After being stirred for 30 min at room temperature the reaction was quenched by the addition of 12 mL of 1M aqueous HCl. The mixture was extracted ethyl acetate (2×40 mL) and the combined organic layers were washed with brine (2×30 mL). The solution was dried over Na2SO4 before being concentrated under reduced pressure. The crude product was used directly in the next reaction without further purification.
Workup
- customwas quenched by the addition of 12 mL of 1M aqueous HCl
- extractionThe mixture was extracted ethyl acetate (2×40 mL)
- washthe combined organic layers were washed with brine (2×30 mL)
- dry with materialThe solution was dried over Na2SO4
- concentrationbefore being concentrated under reduced pressure
- customThe crude product was used directly in the next reaction without further purification
Sources & evidence
- ORD record
- ord-90a8401d79f44b1e9388804b642fe7b0
- Source dataset
- uspto-grants-2011_02
- Patent number
- US07879911B2
Reaction notes
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