Hydrochloric Acid → tert-butyl (3RS,4RS)-3-(naphthalen-2-ylmethoxy)-4-[4-[2-[4-(2-trimethylsilanyl-ethoxy methoxy)-benzoyloxy]-ethoxy]-phenyl]-piperidine-1-carboxylate
Reaction equation
[CH2:55]([N:56]=[C:57]=[N:58][CH2:59][CH2:60][CH2:61][N:62]([CH3:63])[CH3:64])[CH3:65].[CH3:36][Si:37]([CH2:38][CH2:39][O:40][CH2:41][O:42][c:43]1[cH:44][cH:45][c:46]([C:47](=[O:48])[OH:49])[cH:50][cH:51]1)([CH3:52])[CH3:53].[ClH:54].[OH:1][CH2:2][CH2:3][O:4][c:5]1[cH:6][cH:7][c:8]([CH:11]2[CH:12]([O:24][CH2:25][c:26]3[cH:27][c:28]4[cH:29][cH:30][cH:31][cH:32][c:33]4[cH:34][cH:35]3)[CH2:13][N:14]([C:17](=[O:18])[O:19][C:20]([CH3:21])([CH3:22])[CH3:23])[CH2:15][CH2:16]2)[cH:9][cH:10]1>>[O:1]([CH2:2][CH2:3][O:4][c:5]1[cH:6][cH:7][c:8]([CH:11]2[CH:12]([O:24][CH2:25][c:26]3[cH:27][c:28]4[cH:29][cH:30][cH:31][cH:32][c:33]4[cH:34][cH:35]3)[CH2:13][N:14]([C:17](=[O:18])[O:19][C:20]([CH3:21])([CH3:22])[CH3:23])[CH2:15][CH2:16]2)[cH:9][cH:10]1)[C:47]([c:46]1[cH:45][cH:44][c:43]([O:42][CH2:41][O:40][CH2:39][CH2:38][Si:37]([CH3:36])([CH3:52])[CH3:53])[cH:51][cH:50]1)=[O:48]Participants
5
Reactant 4
Product 1
Sources & evidence
- ORD record
- ord-3485a9a57e27466da6b89f45d487be97
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (9/10)
Reaction notes
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