HRID671256

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID8028

Tetrahydrofuran

C4H8O

HCID11776

Triphenylphosphine

C18H15P

HCID118940

tert-Butyl 2-hydroxy-2-methylpropanoate

C8H16O3

HCID165337

Propanoic acid, 2-methyl-, ion(1-)

C4H7O2-

HCID220568

Diethyl azodicarboxylate

C6H10N2O4

HCID3016048

o-(p-Nitrophenoxy)phenol

C12H9NO4

PRODUCTS

生成物

结构：CC(C)(C)OC(=O)C(C)(C)Oc1ccccc1Oc1ccc([N+](=O)[O-])cc1

HCID21025175

未命名化合物

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-add2b1fc2ce84316baf1137b11577a37
来源数据集: Training data from https://doi.org/10.1039/C8SC04228D (3/10)
DOI: 10.1039/C8SC04228D
来源说明: Training data from https://doi.org/10.1039/C8SC04228D (3/10)

反应 SMILES

[CH2:66]1[O:67][CH2:68][CH2:69][CH2:70]1.[CH3:60][CH:61]([C:62](=[O:63])[O-:64])[CH3:65].[N+:1](=[O:2])([O-:3])[c:4]1[cH:5][cH:6][c:7]([O:8][c:9]2[c:10]([OH:15])[cH:11][cH:12][cH:13][cH:14]2)[cH:16][cH:17]1.[O:48]=[C:49]([O:50][CH2:51][CH3:52])[N:53]=[N:54][C:55]([O:56][CH2:57][CH3:58])=[O:59].[OH:37][C:38]([C:39](=[O:40])[O:41][C:42]([CH3:43])([CH3:44])[CH3:45])([CH3:46])[CH3:47].[c:18]1([P:19]([c:20]2[cH:21][cH:22][cH:23][cH:24][cH:25]2)[c:26]2[cH:27][cH:28][cH:29][cH:30][cH:31]2)[cH:32][cH:33][cH:34][cH:35][cH:36]1>>[N+:1](=[O:2])([O-:3])[c:4]1[cH:5][cH:6][c:7]([O:8][c:9]2[c:10]([O:15][C:38]([C:39](=[O:40])[O:41][C:42]([CH3:43])([CH3:44])[CH3:45])([CH3:46])[CH3:47])[cH:11][cH:12][cH:13][cH:14]2)[cH:16][cH:17]1