Benzyl Alcohol → Trifluoromethanesulfonic acid 6-benzyloxy-1-[4-(2-piperidin-1-yl-ethoxy)-phenoxy]-naphthalen-2-yl ester
Reaction equation
[CH3:77][CH2:78][O:79][C:80](=[O:81])[CH3:82].[O:63]=[C:64]([O:65][CH:66]([CH3:67])[CH3:68])[N:69]=[N:70][C:71]([O:72][CH:73]([CH3:74])[CH3:75])=[O:76].[O:83]1[CH2:84][CH2:85][CH2:86][CH2:87]1.[OH:1][c:2]1[cH:3][c:4]2[cH:5][cH:6][c:7]([O:28][S:29](=[O:30])(=[O:31])[C:32]([F:33])([F:34])[F:35])[c:8]([O: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)[c:9]2[cH:10][cH:11]1.[OH:55][CH2:56][c:57]1[cH:58][cH:59][cH:60][cH:61][cH:62]1.[c:36]1([P:37]([c:38]2[cH:39][cH:40][cH:41][cH:42][cH:43]2)[c:44]2[cH:45][cH:46][cH:47][cH:48][cH:49]2)[cH:50][cH:51][cH:52][cH:53][cH:54]1>>[O:1]([c:2]1[cH:3][c:4]2[cH:5][cH:6][c:7]([O:28][S:29](=[O:30])(=[O:31])[C:32]([F:33])([F:34])[F:35])[c:8]([O: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)[c:9]2[cH:10][cH:11]1)[CH2:56][c:57]1[cH:58][cH:59][cH:60][cH:61][cH:62]1Participants
7
Reactant 6
Product 1
Sources & evidence
- ORD record
- ord-aa9d409c844e43d389360e053be95485
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (7/10)
Reaction notes
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