HRID1232717

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID8028

Tetrahydrofuran

C4H8O

HCID10665

1H-Isoindole-1,3(2H)-dione, 2-hydroxy-

C8H5NO3

HCID11776

Triphenylphosphine

C18H15P

HCID220568

Diethyl azodicarboxylate

C6H10N2O4

结构：OCc1cc(Cl)c2c(c1Cl)OC(c1ccccc1)(c1ccccc1)O2

HCID19917989

4,7-Dichloro-2,2-diphenyl-1,3-benzodioxole-5-methanol

C20H14Cl2O3

PRODUCTS

生成物

结构：O=C1c2ccccc2C(=O)N1OCc1cc(Cl)c2c(c1Cl)OC(c1ccccc1)(c1ccccc1)O2

HCID19917897

未命名化合物

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-22baedaba9d94bf193eddff58a5f2aa3
来源数据集: Training data from https://doi.org/10.1039/C8SC04228D (5/10)
DOI: 10.1039/C8SC04228D
来源说明: Training data from https://doi.org/10.1039/C8SC04228D (5/10)

反应 SMILES

[Cl:1][c:2]1[c:3]([CH2:24][OH:25])[cH:4][c:5]([Cl:23])[c:6]2[c:10]1[O:9][C:8]([c:11]1[cH:12][cH:13][cH:14][cH:15][cH:16]1)([c:17]1[cH:18][cH:19][cH:20][cH:21][cH:22]1)[O:7]2.[O:57]=[C:58]([O:59][CH2:60][CH3:61])[N:62]=[N:63][C:64]([O:65][CH2:66][CH3:67])=[O:68].[O:69]1[CH2:70][CH2:71][CH2:72][CH2:73]1.[OH:26][N:27]1[C:28](=[O:37])[c:29]2[c:30]([cH:33][cH:34][cH:35][cH:36]2)[C:31]1=[O:32].[c:38]1([P:39]([c:40]2[cH:41][cH:42][cH:43][cH:44][cH:45]2)[c:46]2[cH:47][cH:48][cH:49][cH:50][cH:51]2)[cH:52][cH:53][cH:54][cH:55][cH:56]1>>[Cl:1][c:2]1[c:3]([CH2:24][O:25][N:27]2[C:28](=[O:37])[c:29]3[c:30]([cH:33][cH:34][cH:35][cH:36]3)[C:31]2=[O:32])[cH:4][c:5]([Cl:23])[c:6]2[c:10]1[O:9][C:8]([c:11]1[cH:12][cH:13][cH:14][cH:15][cH:16]1)([c:17]1[cH:18][cH:19][cH:20][cH:21][cH:22]1)[O:7]2