2-Bromomethylnaphthalene → tert-butyl (3RS,4RS)-4-(4-methoxycarbonyl-phenyl)-3-naphthalen-2-ylmethoxy-piperidine-1-carboxylate

HRID 283145

Reaction equation

HRID 283145 reaction equation
[Br:25][CH2:26][c:27]1[cH:28][c:29]2[cH:30][cH:31][cH:32][cH:33][c:34]2[cH:35][cH:36]1.[OH:1][CH:2]1[CH2:3][N:4]([C:18](=[O:19])[O:20][C:21]([CH3:22])([CH3:23])[CH3:24])[CH2:5][CH2:6][CH:7]1[c:8]1[cH:9][cH:10][c:11]([C:14](=[O:15])[O:16][CH3:17])[cH:12][cH:13]1>>[O:1]([CH:2]1[CH2:3][N:4]([C:18](=[O:19])[O:20][C:21]([CH3:22])([CH3:23])[CH3:24])[CH2:5][CH2:6][CH:7]1[c:8]1[cH:9][cH:10][c:11]([C:14](=[O:15])[O:16][CH3:17])[cH:12][cH:13]1)[CH2:26][c:27]1[cH:28][c:29]2[cH:30][cH:31][cH:32][cH:33][c:34]2[cH:35][cH:36]1

Participants

3

Reactant 2

HCID 703202-BromomethylnaphthaleneHCID 53949513Tert-butyl 3-hydroxy-4-(4-methoxycarbonylphenyl)piperidine-1-carboxylate

Product 1

HCID 54007898tert-butyl (3RS,4RS)-4-(4-methoxycarbonyl-phenyl)-3-naphthalen-2-ylmethoxy-piperidine-1-carboxylate

Sources & evidence

ORD record
ord-39330dace42d40a6a492d7bab1841cff
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (8/10)

Linked notes

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