HRID145656

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

ethyl N-ethoxycarbonyliminocarbamate

C6H10N2O4

结构：CC(C)(C)[Si](OCCCCO)(c1ccccc1)c1ccccc1

HCID10065108

1-Butanol, 4-[[(1,1-dimethylethyl)diphenylsilyl]oxy]-

C20H28O2Si

PRODUCTS

生成物

结构：CC(C)(C)[Si](OCCCCON1C(=O)c2ccccc2C1=O)(c1ccccc1)c1ccccc1

HCID22286313

未命名化合物

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-83fc79409e914b0ba3c31747a21fec9e
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

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