HRID2348482

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID8857

Ethyl acetate

C4H8O2

HCID107909

Phosphorous acid

H3O3P

HCID11322811

1-Cyclohexyloxy-2,2,6,6-tetramethyl-piperidin-4-ol

C15H29NO2

HCID13118721

{2-Hydroxy-4-[(oxiran-2-yl)methoxy]phenyl}(phenyl)methanone

C16H14O4

PRODUCTS

生成物

结构：CC1(C)CC(OCC(O)COc2ccc(C(=O)c3ccccc3)c(O)c2)CC(C)(C)N1OC1CCCCC1

HCID53690550

未命名化合物

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-115c64b00fec4a8988862709f018ca87
来源数据集: Training data from https://doi.org/10.1039/C8SC04228D (10/10)
DOI: 10.1039/C8SC04228D
来源说明: Training data from https://doi.org/10.1039/C8SC04228D (10/10)

反应 SMILES

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