4-Hydroxybenzaldehyde → tert-Butyl 2-(4-formylphenoxy)-2-methylpropanoate

Reaktionsgleichung

[Br:16][C:17]([C:18](=[O:19])[O:20][C:21]([CH3:22])([CH3:23])[CH3:24])([CH3:25])[CH3:26].[C:10](=[O:11])([O-:12])[O-:13].[CH3:28][N:29]([CH3:30])[CH:31]=[O:32].[K+:14].[K+:15].[OH2:27].[OH:1][c:2]1[cH:3][cH:4][c:5]([CH:6]=[O:7])[cH:8][cH:9]1>>[O:1]([c:2]1[cH:3][cH:4][c:5]([CH:6]=[O:7])[cH:8][cH:9]1)[C:17]([C:18](=[O:19])[O:20][C:21]([CH3:22])([CH3:23])[CH3:24])([CH3:25])[CH3:26]

Komponenten

Edukt 6

HCID 1264-Hydroxybenzaldehyde

HCID 813Potassium Cation2×

HCID 962Water

HCID 6228Dimethylformamide

HCID 19660Carbonate Ion

HCID 90290tert-Butyl 2-bromo-2-methylpropionate

Produkt 1

HCID 22708193tert-Butyl 2-(4-formylphenoxy)-2-methylpropanoate

Quellen und Nachweise

ORD-Eintrag: ord-bd091d0c79d94c6387866ee801ddcae1
Quelldatensatz: Training data from https://doi.org/10.1039/C8SC04228D (8/10)
DOI: 10.1039/C8SC04228D

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