3-(3,4-Dimethoxyphenyl)-4,4-diethoxy-2-ethoxycarbonylbutyric acid ethyl ester → 4,4-Diethoxy-3-[4-methoxy-3-(2-methylpropoxy)phenyl]butyric acid

HRID 1977697Notes

Reaction equation

HRID 1977697 reaction equation
C([O:3][C:4](=[O:32])[CH:5](C(OCC)=O)[CH:6]([C:14]1[CH:19]=[CH:18][C:17]([O:20][CH3:21])=[C:16]([O:22][CH2:23][CH:24]([CH3:26])[CH3:25])[CH:15]=1)[CH:7]([O:11][CH2:12][CH3:13])[O:8][CH2:9][CH3:10])C.C(OC(=O)C(C(OCC)=O)C(C1C=CC(OC)=C(OC)C=1)C(OCC)OCC)C>>[CH2:9]([O:8][CH:7]([O:11][CH2:12][CH3:13])[CH:6]([C:14]1[CH:19]=[CH:18][C:17]([O:20][CH3:21])=[C:16]([O:22][CH2:23][CH:24]([CH3:25])[CH3:26])[CH:15]=1)[CH2:5][C:4]([OH:32])=[O:3])[CH3:10]

Participants

3

Reactant 2

HCID 155213723-(3,4-Dimethoxyphenyl)-4,4-diethoxy-2-ethoxycarbonylbutyric acid ethyl esterHCID 219945274,4-Diethoxy-2-ethoxycarbonyl-3-[4-methoxy-3-(2-methylpropoxy)phenyl]butyric acid ethyl ester

Product 1

HCID 219945194,4-Diethoxy-3-[4-methoxy-3-(2-methylpropoxy)phenyl]butyric acidYield 48.6%

Procedure

Using the same procedure as in Example 1 (3), 4,4-diethoxy-2-ethoxycarbonyl-3-[4-methoxy-3-(2-methylpropoxy)phenyl]butyric acid ethyl ester, instead of 3-(3,4-dimethoxyphenyl)-4,4-diethoxy-2-ethoxycarbonylbutyric acid ethyl ester, was used to obtain a light yellow solid of the above-described compound via 4,4-diethoxy-3-[4-methoxy-3-(2-methylpropoxy)phenyl]butyric acid (yield 48.6%).

Sources & evidence

ORD record
ord-2baddca866134456bc557431e2c23a2a
Source dataset
uspto-grants-2001_05
Patent number
US06235739B1

Reaction notes

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