HRID2141741

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID5943

Carbon tetrachloride

CCl4

HCID7187

Benzoyl peroxide

C14H10O4

HCID19165

1-Methyl-3-phenoxybenzene

C13H12O

HCID67184

1-Bromopyrrolidine-2,5-dione

C4H4BrNO2

结构：CN(Cc1ccc(C(C)(C)C)cc1)Cc1cccc(Oc2ccccc2)c1

HCID23286207

未命名化合物

PRODUCTS

生成物

HCID94544

1-(Bromomethyl)-3-phenoxybenzene

C13H11BrO

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-8cf2b81e2e5d4e0a9964d2df4d07687e
来源数据集: Training data from https://doi.org/10.1039/C8SC04228D (4/10)
DOI: 10.1039/C8SC04228D
来源说明: Training data from https://doi.org/10.1039/C8SC04228D (4/10)

反应 SMILES

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