O-Xylene → HCID 22503481, compound
Reaction equation
[Br:29][c:30]1[n:31][c:32]([N:40]2[CH2:41][CH2:42][N:43]([CH2:46][CH3:47])[CH2:44][CH2:45]2)[c:33]2[cH:34][cH:35][cH:36][cH:37][c:38]2[cH:39]1.[C:1]([CH3:2])(=[O:3])[O:4][CH2:5][CH2:6][C:7]([CH3:8])([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)[CH3:28].[CH3:56][CH2:57][O:58][C:59](=[O:60])[CH3:61].[c:48]1([CH3:49])[c:50]([CH3:51])[cH:52][cH:53][cH:54][cH:55]1>>[C:1]([CH3:2])(=[O:3])[O:4][CH2:5][CH2:6][C:7]([CH3:8])([c:9]1[cH:10][cH:11][c:12](-[c:30]2[n:31][c:32]([N:40]3[CH2:41][CH2:42][N:43]([CH2:46][CH3:47])[CH2:44][CH2:45]3)[c:33]3[cH:34][cH:35][cH:36][cH:37][c:38]3[cH:39]2)[cH:13][cH:14]1)[CH3:28]Participants
5
Sources & evidence
- ORD record
- ord-c3df258a5c074d44bb0f4574d6679030
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (4/10)
Reaction notes
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