Chloride → 2-(4-Acetoxybenzoylamino)-4-octylphenol
Reaction equation
[C:2]([CH3:3])(=[O:4])[O:5][c:6]1[cH:7][cH:8][c:9]([C:10](=[O:11])[OH:12])[cH:13][cH:14]1.[Cl-:1].[NH2:15][c:16]1[c:17]([OH:30])[cH:18][cH:19][c:20]([CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH3:29])[cH:21]1.[O:31]1[CH2:32][CH2:33][O:34][CH2:35][CH2:36]1.[OH2:43].[cH:37]1[cH:38][cH:39][n:40][cH:41][cH:42]1>>[C:2]([CH3:3])(=[O:4])[O:5][c:6]1[cH:7][cH:8][c:9]([C:10](=[O:12])[NH:15][c:16]2[c:17]([OH:30])[cH:18][cH:19][c:20]([CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH3:29])[cH:21]2)[cH:13][cH:14]1Participants
7
Sources & evidence
- ORD record
- ord-7eb6adcdc6cb49688addb68a0a27ff4e
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (5/10)
Reaction notes
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