4-(2,3-Dichloro-4-valerylphenoxy)butyric acid → 4-[2,3-Dichloro-4-(2-methylenevaleryl)phenoxy]butyric acid

HRID 255933Notes

Reaction equation

HRID 255933 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

Reactant 2

HCID 139587344-(2,3-Dichloro-4-valerylphenoxy)butyric acidHCID 140998584-(2,3-Dichloro-4-butyrylphenoxy)butyric acid

Product 1

HCID 139587354-[2,3-Dichloro-4-(2-methylenevaleryl)phenoxy]butyric acid

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

  1. customthe reaction

Sources & evidence

ORD record
ord-f20658f56f154fd08bffca166c736ddc
Source dataset
uspto-grants-1987_10
Patent number
US04699926

Reaction notes

Loading…