Reaction equation
[O:1]([C:8]1[CH:9]=[C:10]([OH:14])[CH:11]=[CH:12][CH:13]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH3:15][C:16]([CH3:18])=[O:17].[OH:19][C:20]1C=CC(C(OCC)=O)=C[CH:21]=1.[CH3:31]C(CC)=O>>[O:1]([C:8]1[CH:9]=[C:10]([CH:11]=[CH:12][CH:13]=1)[O:14][CH2:21][C:20]([O:17][C:16]([CH3:31])([CH3:18])[CH3:15])=[O:19])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1Participants
5
Procedure
t-Butyl (3-phenoxy)phenoxyacetate was prepared following the alkylation procedure as described in example 66 using 3-phenoxyphenol and acetone in lieu of ethyl 4-hydroxybenzoate and methylethylketone.
Sources & evidence
- ORD record
- ord-aa48b40aad0d42c8961e7bbe9fc0f157
- Source dataset
- uspto-grants-1993_05
- Patent number
- US05214204
Linked notes
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