HRID946545

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID7912

Diisopropylamine

C6H15N

HCID8028

Tetrahydrofuran

C4H8O

HCID8058

n-Hexane

C6H14

HCID8857

Ethyl acetate

C4H8O2

HCID205808

Propanoic acid, 2-(4-cyanophenoxy)-2-methyl-, ethyl ester

C13H15NO3

HCID12397252

5-(Benzyloxy)-2-methyl-1-oxo-1lambda~5~-pyridine

C13H13NO2

HCID178418339

未命名化合物

PRODUCTS

生成物

结构：CC(C)(Oc1ccc(C#N)cc1)C(=O)Cc1ccc(OCc2ccccc2)c[n+]1[O-]

HCID54393238

未命名化合物

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-157581ffc2f34b9eb7e0e499875c6a47
来源数据集: Validation data from https://doi.org/10.1039/C8SC04228D
DOI: 10.1039/C8SC04228D
来源说明: Validation data from https://doi.org/10.1039/C8SC04228D

反应 SMILES

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