Potassium Cation → 3-(4-Bromo-2-formyl-phenoxy)-2,2-dimethyl-propionic acid methyl ester

Reaktionsgleichung

[Br:1][c:2]1[cH:3][cH:4][c:5]([OH:10])[c:6]([CH:7]=[O:8])[cH:9]1.[CH3:11][O:12][C:13]([C:14]([CH2:15][O:16][S:17]([c:18]1[cH:19][cH:20][c:21]([CH3:22])[cH:23][cH:24]1)(=[O:25])=[O:26])([CH3:27])[CH3:28])=[O:29].[K+:30].[K+:31].[O-:32][C:33]([O-:34])=[O:35].[O:36]=[CH:37][N:38]([CH3:39])[CH3:40]>>[Br:1][c:2]1[cH:3][cH:4][c:5]([O:10][CH2:15][C:14]([C:13]([O:12][CH3:11])=[O:29])([CH3:27])[CH3:28])[c:6]([CH:7]=[O:8])[cH:9]1

Komponenten

Edukt 5

HCID 813Potassium Cation2×

HCID 6228Dimethylformamide

HCID 19660Carbonate Ion

HCID 728635-Bromosalicylaldehyde

HCID 22479327Methyl 3-(p-tolylsulfonyloxy)-2,2-dimethylpropanoate

Produkt 1

HCID 575659193-(4-Bromo-2-formyl-phenoxy)-2,2-dimethyl-propionic acid methyl ester

Quellen und Nachweise

ORD-Eintrag: ord-0297a4fdc4724e7b9c51395d75091355
Quelldatensatz: Training data from https://doi.org/10.1039/C8SC04228D (10/10)
DOI: 10.1039/C8SC04228D

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