O-Xylene → HCID 22132659, compound

HRID 316979Notes

Reaction equation

HRID 316979 reaction equation
[CH3:33][N:34]([CH3:35])[c:36]1[cH:37][cH:38][n:39][cH:40][cH:41]1.[Cl:18][c:19]1[cH:20][cH:21][n:22][c:23]2[cH:24][c:25]([O:31][CH3:32])[c:26]([O:29][CH3:30])[cH:27][c:28]12.[OH:1][c:2]1[cH:3][cH:4][c:5]([C:8](=[O:9])[c:10]2[cH:11][c:12]([Cl:17])[c:13]([Cl:16])[cH:14][cH:15]2)[cH:6][cH:7]1.[c:42]1([CH3:43])[c:44]([CH3:45])[cH:46][cH:47][cH:48][cH:49]1>>[O:1]([c:2]1[cH:3][cH:4][c:5]([C:8](=[O:9])[c:10]2[cH:11][c:12]([Cl:17])[c:13]([Cl:16])[cH:14][cH:15]2)[cH:6][cH:7]1)[c:19]1[cH:20][cH:21][n:22][c:23]2[cH:24][c:25]([O:31][CH3:32])[c:26]([O:29][CH3:30])[cH:27][c:28]12

Participants

5

Reactant 4

HCID 7237O-XyleneHCID 142844-(Dimethylamino)pyridineHCID 4596104-Chloro-6,7-dimethoxyquinolineHCID 12299673(3,4-Dichlorophenyl)(4-hydroxyphenyl)methanone

Product 1

HCID 22132659HCID 22132659, compound

Sources & evidence

ORD record
ord-4c615b72f81341189e9d3739b561d2fe
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (8/10)

Reaction notes

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