Benzyl Alcohol → Trifluoromethanesulfonic acid 6-benzyloxy-1-[4-(2-piperidin-1-yl-ethoxy)-benzoyl]-naphthalen-2-yl ester
Reaction equation
[CH2:59]1[O:60][CH2:61][CH2:62][CH2:63]1.[O:45]=[C:46]([O:47][CH:48]([CH3:49])[CH3:50])[N:51]=[N:52][C:53]([O:54][CH:55]([CH3:56])[CH3:57])=[O:58].[OH:1][c:2]1[cH:3][c:4]2[cH:5][cH:6][c:7]([O:29][S:30](=[O:31])(=[O:32])[C:33]([F:34])([F:35])[F:36])[c:8]([C:12]([c:13]3[cH:14][cH:15][c:16]([O:19][CH2:20][CH2:21][N:22]4[CH2:23][CH2:24][CH2:25][CH2:26][CH2:27]4)[cH:17][cH:18]3)=[O:28])[c:9]2[cH:10][cH:11]1.[OH:37][CH2:38][c:39]1[cH:40][cH:41][cH:42][cH:43][cH:44]1>>[O:1]([c:2]1[cH:3][c:4]2[cH:5][cH:6][c:7]([O:29][S:30](=[O:31])(=[O:32])[C:33]([F:34])([F:35])[F:36])[c:8]([C:12]([c:13]3[cH:14][cH:15][c:16]([O:19][CH2:20][CH2:21][N:22]4[CH2:23][CH2:24][CH2:25][CH2:26][CH2:27]4)[cH:17][cH:18]3)=[O:28])[c:9]2[cH:10][cH:11]1)[CH2:38][c:39]1[cH:40][cH:41][cH:42][cH:43][cH:44]1Participants
5
Reactant 4
Product 1
Sources & evidence
- ORD record
- ord-7e9f37622cf5463995fd33ea9f735d15
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (7/10)
Reaction notes
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