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Hydroxide → [3-(4-chlorobenzyl)-2,4,7-trimethylquinolin-5-yloxy]acetic Acid

HRID 299222
Notes
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Reaction equation

HRID 299222 reaction equation
[CH3:1][O:2][C:3]([CH2:4][O:5][c:6]1[c:7]2[c:8]([CH3:26])[c:9]([CH2:18][c:19]3[cH:20][cH:21][c:22]([Cl:25])[cH:23][cH:24]3)[c:10]([CH3:17])[n:11][c:12]2[cH:13][c:14]([CH3:16])[cH:15]1)=[O:27].[CH3:28][C:29]#[N:30].[Li+:31].[O:33]1[CH2:34][CH2:35][CH2:36][CH2:37]1.[OH-:32]>>[O:2]=[C:3]([CH2:4][O:5][c:6]1[c:7]2[c:8]([CH3:26])[c:9]([CH2:18][c:19]3[cH:20][cH:21][c:22]([Cl:25])[cH:23][cH:24]3)[c:10]([CH3:17])[n:11][c:12]2[cH:13][c:14]([CH3:16])[cH:15]1)[OH:27]
ParticipantsSources & evidenceReaction notes

Participants

6

Reactant 5

HCID 961HydroxideHCID 6342AcetonitrileHCID 8028TetrahydrofuranHCID 28486Lithium ionHCID 68782119[3-(4-chlorobenzyl)-2,4,7-trimethylquinolin-5-yloxy]acetic Acid Methyl Ester

Product 1

HCID 57742515[3-(4-chlorobenzyl)-2,4,7-trimethylquinolin-5-yloxy]acetic Acid

Sources & evidence

ORD record
ord-ac82ea30126a4d0894617d647a02abec
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (8/10)
DOI
10.1039/C8SC04228D

Reaction notes

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On this pageParticipantsSources & evidenceReaction notes