O-Xylene → HCID 22502478, compound
Reaction equation
[Br:28][c:29]1[n:30][c:31]([N:39]2[CH2:40][CH2:41][N:42]([CH2:45][CH3:46])[CH2:43][CH2:44]2)[c:32]2[cH:33][cH:34][cH:35][cH:36][c:37]2[cH:38]1.[CH3:1][O:2][CH2:3][CH2:4][CH2:5][S:6](=[O:7])(=[O:8])[c:9]1[cH:10][cH:11][c:12]([Sn:15]([CH2:16][CH2:17][CH2:18][CH3:19])([CH2:20][CH2:21][CH2:22][CH3:23])[CH2:24][CH2:25][CH2:26][CH3:27])[cH:13][cH:14]1.[CH3:55][CH2:56][O:57][C:58](=[O:59])[CH3:60].[c:47]1([CH3:48])[c:49]([CH3:50])[cH:51][cH:52][cH:53][cH:54]1>>[CH3:1][O:2][CH2:3][CH2:4][CH2:5][S:6](=[O:7])(=[O:8])[c:9]1[cH:10][cH:11][c:12](-[c:29]2[n:30][c:31]([N:39]3[CH2:40][CH2:41][N:42]([CH2:45][CH3:46])[CH2:43][CH2:44]3)[c:32]3[cH:33][cH:34][cH:35][cH:36][c:37]3[cH:38]2)[cH:13][cH:14]1Participants
5
Sources & evidence
- ORD record
- ord-3de7b9e0edeb45c3a470215fb2359b90
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (4/10)
Reaction notes
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