Water → {3-[4-Chloro-2-(2-oxo-oxazolidin-3-ylmethyl)-phenoxy]-4-methoxy-phenyl}-acetic acid

HRID 885374Notes

Reaction equation

HRID 885374 reaction equation
C([O:3][C:4](=[O:29])[CH2:5][C:6]1[CH:11]=[CH:10][C:9]([O:12][CH3:13])=[C:8]([O:14][C:15]2[CH:20]=[CH:19][C:18]([Cl:21])=[CH:17][C:16]=2[CH2:22][N:23]2[CH2:27][CH2:26][O:25][C:24]2=[O:28])[CH:7]=1)C.[OH-].[Li+].O>O1CCOCC1>[Cl:21][C:18]1[CH:19]=[CH:20][C:15]([O:14][C:8]2[CH:7]=[C:6]([CH2:5][C:4]([OH:29])=[O:3])[CH:11]=[CH:10][C:9]=2[O:12][CH3:13])=[C:16]([CH2:22][N:23]2[CH2:27][CH2:26][O:25][C:24]2=[O:28])[CH:17]=1

Participants

5

Reactant 3

HCID 962WaterHCID 3939Lithium HydroxideHCID 58237617{3-[4-Chloro-2-(2-oxo-oxazolidin-3-ylmethyl)-phenoxy]-4-methoxy-phenyl}-acetic acid ethyl ester

Product 1

HCID 44187348{3-[4-Chloro-2-(2-oxo-oxazolidin-3-ylmethyl)-phenoxy]-4-methoxy-phenyl}-acetic acid

Reagents, catalysts & solvents 1

HCID 312751,4-DioxaneSolvent

Procedure

To {3-[4-chloro-2-(2-oxo-oxazolidin-3-ylmethyl)-phenoxy]-4-methoxy-phenyl}-acetic acid ethyl ester (0.36 mmol) in 1,4-dioxane was added lithium hydroxide and H2O, and the reaction was stirred overnight at room temperature. The mixture was worked-up, and the residue was purified by preparative HPLC to give the title compound.

Workup

  1. customthe residue was purified by preparative HPLC

Sources & evidence

ORD record
ord-f75deee3b011487fad3e45fef59eaecb
Source dataset
uspto-grants-2012_08
Patent number
US08242145B2

Reaction notes

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