Acetate → 2-Chloro-3-(2,2,4-trimethyl-1,2-dihydroquinolin-6-yl)-phenol

Reaktionsgleichung

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

Komponenten

Edukt 4

HCID 175Acetate

HCID 813Potassium Cation

HCID 113798142-Chloro-3-iodophenol

HCID 225665302,2,4-Trimethyl-6-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-1,2-dihydroquinoline

Produkt 1

HCID 225665412-Chloro-3-(2,2,4-trimethyl-1,2-dihydroquinolin-6-yl)-phenol

Quellen und Nachweise

ORD-Eintrag: ord-878fc60112974e99b3451f0d55ae6e20
Quelldatensatz: Training data from https://doi.org/10.1039/C8SC04228D (7/10)
DOI: 10.1039/C8SC04228D

Notizen zur Reaktion

Wird geladen…