聚[6-[4-(4-氰基苯基)苯氧基]己基甲基丙烯酸酯] → 2-(N-Boc-piperidine-4-yloxy)-4-(tert-butyl)benzoic acid

反应方程式

[C:1]([CH3:2])([CH3:3])([CH3:4])[O:5][C:6](=[O:7])[N:8]1[CH2:9][CH2:10][CH:11]([O:14][c:15]2[c:16]([C:17](=[O:18])[O:19][CH3:20])[cH:21][cH:22][c:23]([C:25]([CH3:26])([CH3:27])[CH3:28])[cH:24]2)[CH2:12][CH2:13]1.[OH2:29]>>[C:1]([CH3:2])([CH3:3])([CH3:4])[O:5][C:6](=[O:7])[N:8]1[CH2:9][CH2:10][CH:11]([O:14][c:15]2[c:16]([C:17](=[O:18])[OH:19])[cH:21][cH:22][c:23]([C:25]([CH3:26])([CH3:27])[CH3:28])[cH:24]2)[CH2:12][CH2:13]1

参与物

反应物 2

HCID 962聚[6-[4-(4-氰基苯基)苯氧基]己基甲基丙烯酸酯]

HCID 68532357methyl 4-(tert-butyl)-2-(1-Boc-piperidin-4-yloxy)benzoate

产物 1

HCID 685305052-(N-Boc-piperidine-4-yloxy)-4-(tert-butyl)benzoic acid

来源与证据

ORD记录: ord-dd54964266ff48e0a11f72a53dbeb3bd
来源数据集: Training data from https://doi.org/10.1039/C8SC04228D (5/10)
DOI: 10.1039/C8SC04228D

反应笔记

加载中…