4-(2,3-Dichloro-4-valerylphenoxy)butyric acid → 4-[2,3-Dichloro-4-(2-methylenevaleryl)phenoxy]butyric acid
Reaction equation
[Cl:1][C:2]1[C:14]([Cl:15])=[C:13]([C:16](=[O:21])[CH2:17][CH2:18][CH2:19][CH3:20])[CH:12]=[CH:11][C:3]=1[O:4][CH2:5][CH2:6][CH2:7][C:8]([OH:10])=[O:9].Cl[C:23]1C(Cl)=C(C(=O)CCC)C=CC=1OCCCC(O)=O>>[Cl:1][C:2]1[C:14]([Cl:15])=[C:13]([C:16](=[O:21])[C:17](=[CH2:23])[CH2:18][CH2:19][CH3:20])[CH:12]=[CH:11][C:3]=1[O:4][CH2:5][CH2:6][CH2:7][C:8]([OH:10])=[O:9]Participants
3
Procedure
By conducting the reaction as described in Example 2, Step B, except that an equimolar amount of 4-(2,3-dichloro-4-valerylphenoxy)butyric acid was substituted for the 4-(2,3-dichloro-4-butyrylphenoxy)butyric acid, there was obtained 4-[2,3-dichloro-4-(2-methylenevaleryl)phenoxy]butyric acid, m.p. 85°-87° C.
Workup
- customthe reaction
Sources & evidence
- ORD record
- ord-901ff9d7751c41cb85a4133799c6841a
- Source dataset
- uspto-grants-1988_03
- Patent number
- US04731473
Reaction notes
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