HRID2146550

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID5943

Carbon tetrachloride

CCl4

HCID7187

Benzoyl peroxide

C14H10O4

HCID67184

1-Bromopyrrolidine-2,5-dione

C4H4BrNO2

结构：CC(=O)OC1CCC2(C)C(CCC3C2CCC2(C)C(C(C)=O)CCC32)C1

HCID296381

20-Oxopregnan-3-yl acetate

C23H36O3

PRODUCTS

生成物

结构：CC(=O)OC1CCC2(C)C(CCC3C2CCC2(C)C3CCC2(Br)C(C)=O)C1

HCID538107

未命名化合物

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-ada71d1c839a47219f007cc36c820ec9
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:27][N:28]1[C:29](=[O:30])[CH2:31][CH2:32][C:33]1=[O:34].[C:1]([CH3:2])(=[O:3])[O:4][CH:5]1[CH2:6][CH:7]2[CH2:8][CH2:9][CH:10]3[CH:11]4[CH2:12][CH2:13][CH:14]([C:15]([CH3:16])=[O:17])[C:18]4([CH3:26])[CH2:19][CH2:20][CH:21]3[C:22]2([CH3:25])[CH2:23][CH2:24]1.[C:35]([O:36][O:37][C:38](=[O:39])[c:40]1[cH:41][cH:42][cH:43][cH:44][cH:45]1)(=[O:46])[c:47]1[cH:48][cH:49][cH:50][cH:51][cH:52]1.[C:53]([Cl:54])([Cl:55])([Cl:56])[Cl:57]>>[C:1]([CH3:2])(=[O:3])[O:4][CH:5]1[CH2:6][CH:7]2[CH2:8][CH2:9][CH:10]3[CH:11]4[CH2:12][CH2:13][C:14]([C:15]([CH3:16])=[O:17])([Br:27])[C:18]4([CH3:26])[CH2:19][CH2:20][CH:21]3[C:22]2([CH3:25])[CH2:23][CH2:24]1