O-Xylene → HCID 22503411, compound
Reaction equation
[Br:33][c:34]1[n:35][c:36]([N:44]2[CH2:45][CH2:46][N:47]([CH2:50][CH3:51])[CH2:48][CH2:49]2)[c:37]2[cH:38][cH:39][cH:40][cH:41][c:42]2[cH:43]1.[CH2:1]([c:2]1[cH:3][cH:4][cH:5][cH:6][cH:7]1)[O:8][CH2:9][CH2:10][NH:11][C:12]([c:13]1[cH:14][cH:15][c:16]([Sn:19]([CH2:20][CH2:21][CH2:22][CH3:23])([CH2:24][CH2:25][CH2:26][CH3:27])[CH2:28][CH2:29][CH2:30][CH3:31])[cH:17][cH:18]1)=[O:32].[c:52]1([CH3:53])[c:54]([CH3:55])[cH:56][cH:57][cH:58][cH:59]1>>[CH2:1]([c:2]1[cH:3][cH:4][cH:5][cH:6][cH:7]1)[O:8][CH2:9][CH2:10][NH:11][C:12]([c:13]1[cH:14][cH:15][c:16](-[c:34]2[n:35][c:36]([N:44]3[CH2:45][CH2:46][N:47]([CH2:50][CH3:51])[CH2:48][CH2:49]3)[c:37]3[cH:38][cH:39][cH:40][cH:41][c:42]3[cH:43]2)[cH:17][cH:18]1)=[O:32]Participants
4
Sources & evidence
- ORD record
- ord-c51eb384e16e4586a9d7743dbb54a6ac
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (7/10)
Reaction notes
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