Triethylamine → Diisopropyl P-[[(2-chloro-6-methylphenyl)sulfonyloxy]methyl]phosphonate

Reaktionsgleichung

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

Komponenten

Edukt 4

HCID 8471Triethylamine

HCID 8857Ethyl Acetate

HCID 10867235Diisopropyl hydroxymethylphosphonate

HCID 157253702-Chloro-6-methylbenzene-1-sulfonyl chloride

Produkt 1

HCID 18981636Diisopropyl P-[[(2-chloro-6-methylphenyl)sulfonyloxy]methyl]phosphonate

Quellen und Nachweise

ORD-Eintrag: ord-77aea3bb43d94d20b39710c9aa14e68a
Quelldatensatz: Training data from https://doi.org/10.1039/C8SC04228D (4/10)
DOI: 10.1039/C8SC04228D

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