O-Xylene → HCID 22132765, compound

HRID 321761Notes

Reaction equation

HRID 321761 reaction equation
[CH3:1][c:2]1[c:3]([C:8](=[O:9])[c:10]2[cH:11][cH:12][c:13]([OH:16])[cH:14][cH:15]2)[cH:4][cH:5][cH:6][cH:7]1.[CH3:32][N:33]([CH3:34])[c:35]1[cH:36][cH:37][n:38][cH:39][cH:40]1.[Cl:17][c:18]1[cH:19][cH:20][n:21][c:22]2[cH:23][c:24]([O:30][CH3:31])[c:25]([O:28][CH3:29])[cH:26][c:27]12.[c:41]1([CH3:42])[c:43]([CH3:44])[cH:45][cH:46][cH:47][cH:48]1>>[CH3:1][c:2]1[c:3]([C:8](=[O:9])[c:10]2[cH:11][cH:12][c:13]([O:16][c:18]3[cH:19][cH:20][n:21][c:22]4[cH:23][c:24]([O:30][CH3:31])[c:25]([O:28][CH3:29])[cH:26][c:27]34)[cH:14][cH:15]2)[cH:4][cH:5][cH:6][cH:7]1

Participants

5

Reactant 4

HCID 7237O-XyleneHCID 142844-(Dimethylamino)pyridineHCID 4596104-Chloro-6,7-dimethoxyquinolineHCID 22132708(4-Hydroxyphenyl)(2-methylphenyl)methanone

Product 1

HCID 22132765HCID 22132765, compound

Sources & evidence

ORD record
ord-b766fe7336ed4929b612a4eb1dee61c5
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (8/10)

Reaction notes

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