Ethyl 2-ethoxy-3-(4-hydroxyphenyl)propanoate → HCID 54391311, compound

HRID 987245Notes

Reaction equation

HRID 987245 reaction equation
[CH2:1]([O:3][C:4](=[O:17])[CH:5]([O:14][CH2:15][CH3:16])[CH2:6][C:7]1[CH:12]=[CH:11][C:10]([OH:13])=[CH:9][CH:8]=1)[CH3:2].[CH3:18][S:19]([O:22][C:23]1[CH:24]=[C:25]([CH2:29][CH2:30]CS([O-])(=O)=O)[CH:26]=[CH:27][CH:28]=1)(=[O:21])=[O:20]>>[CH2:1]([O:3][C:4](=[O:17])[CH:5]([O:14][CH2:15][CH3:16])[CH2:6][C:7]1[CH:8]=[CH:9][C:10]([O:13][CH2:30][CH2:29][C:25]2[CH:26]=[CH:27][CH:28]=[C:23]([O:22][S:19]([CH3:18])(=[O:20])=[O:21])[CH:24]=2)=[CH:11][CH:12]=1)[CH3:2]

Participants

3

Reactant 2

HCID 11791243Ethyl 2-ethoxy-3-(4-hydroxyphenyl)propanoateHCID 22988752HCID 22988752, compound

Product 1

HCID 54391311HCID 54391311, compound

Procedure

2-Ethoxy-3-{4-[2-(3-methanesulfonyloxyphenyl)ethoxy]phenyl}propanoic acid ethyl ester was synthesized using the same method as in example 1(b) from 2-ethoxy-3-(4-hydroxyphenyl)propanoic acid ethyl ester (described in Example 20b) and 2-(3-methanesulfonyloxyphenyl)-ethylmethanesulfonate.

Sources & evidence

ORD record
ord-51e8657c3f8c49239615bd7893b57e82
Source dataset
uspto-grants-2003_10
Patent number
US06630600B1

Reaction notes

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