HCID 54279774, compound → HCID 19004421, compound
Reaction equation
C[O:2][C:3](=[O:22])[C:4](=[O:21])[C:5]1[CH:10]=[CH:9][C:8]([O:11][CH2:12][CH2:13][O:14][C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)=[CH:7][CH:6]=1>CO.[OH-].[Na+]>[O:21]=[C:4]([C:5]1[CH:10]=[CH:9][C:8]([O:11][CH2:12][CH2:13][O:14][C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)=[CH:7][CH:6]=1)[C:3]([OH:22])=[O:2]Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
A mixture of alpha-oxo-4-(2-phenoxyethoxy)benzeneacetic acid methyl ester (1.6 g) in methanol (10 mL) and 0.5N sodium hydroxide (30 mL) was treated as in Example 19. Extraction provided solids which were crystallized from diethyl ether-hexane to give 1.4 g of colorless alpha-oxo-4-[[2-(phenoxy)ethyl]oxy]benzeneacetic acid, mp 102°-103° C.
Workup
- additionwas treated as in Example 19
- extractionExtraction
- customprovided solids which
- customwere crystallized from diethyl ether-hexane
Sources & evidence
- ORD record
- ord-f0c40757af7b42a892714f5b5e2619d4
- Source dataset
- uspto-grants-1994_09
- Patent number
- US05344843
Reaction notes
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