HRID168902

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID313

Hydrochloric Acid

ClH

HCID887

Methanol

CH4O

HCID1049

Pyridine

C5H5N

HCID8028

Tetrahydrofuran

C4H8O

结构：C=Cc1c(OC)ccc2cc(C(O)(c3cn(C(c4ccccc4)(c4ccccc4)c4ccccc4)cn3)C(C)C)ccc12

HCID22018366

1-(5-Ethenyl-6-methoxynaphthalen-2-yl)-1-(1-trityl-1H-imidazol-4-yl)-2-methyl-1-propanol

C39H36N2O2

PRODUCTS

生成物

结构：C=Cc1c(OC)ccc2cc(C(O)(c3c[nH]cn3)C(C)C)ccc12

HCID178437261

未命名化合物

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-694d60547a0c4db3afd82369edda3fe2
来源数据集: Training data from https://doi.org/10.1039/C8SC04228D (9/10)
DOI: 10.1039/C8SC04228D
来源说明: Training data from https://doi.org/10.1039/C8SC04228D (9/10)

反应 SMILES

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