HRID119352

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID8028

Tetrahydrofuran

C4H8O

HCID8857

Ethyl acetate

C4H8O2

HCID15096

Tributyltin chloride

C12H27ClSn

HCID59596016

2-[Tri(propan-2-yl)silyl]-1,3-oxazole

C12H23NOSi

HCID178418306

未命名化合物

PRODUCTS

生成物

结构：CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)[c]1cnc([Si](C(C)C)(C(C)C)C(C)C)o1

HCID11497195

5-(tributylstannyl)-2-(triisopropylsilyl)-1,3-oxazole

C24H49NOSiSn

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-f8449e80042a44a2834b7ff1e0970e1b
来源数据集: Training data from https://doi.org/10.1039/C8SC04228D (2/10)
DOI: 10.1039/C8SC04228D
来源说明: Training data from https://doi.org/10.1039/C8SC04228D (2/10)

反应 SMILES

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