Dimethyl Sulfoxide → Acifluorfen-methyl

Reaktionsgleichung

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

Komponenten

Edukt 5

HCID 679Dimethyl Sulfoxide

HCID 813Potassium Cation2×

HCID 19660Carbonate Ion

HCID 171018Methyl 5-chloro-2-nitrobenzoate

HCID 27366032-Chloro-4-(trifluoromethyl)phenol

Produkt 1

HCID 91642Acifluorfen-methyl

Quellen und Nachweise

ORD-Eintrag: ord-0c702018cd5c48f7961f8d40b81f55b0
Quelldatensatz: Training data from https://doi.org/10.1039/C8SC04228D (1/10)
DOI: 10.1039/C8SC04228D

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