HRID909831

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID31235

N-(2-Hydroxyethyl)aniline

C8H11NO

结构：OB(c1ccccc1)C(OC(B(O)c1ccccc1)c1ccccc1)c1ccccc1

HCID67392963

未命名化合物

PRODUCTS

生成物

结构：c1ccc(NCCOB(c2ccccc2)C(OC(B(OCCNc2ccccc2)c2ccccc2)c2ccccc2)c2ccccc2)cc1

HCID67392970

未命名化合物

AUXILIARIES

试剂、催化剂与溶剂

溶剂HCID702

Ethanol

C2H6O

PROCEDURE

实验过程

The entitled compound (43 mg) was obtained by allowing 40.6 mg of bis(4,4′-(phenylhydroxyboryl)benzyl) ether and 14 mg of phenylglycinol to act in 1 mL of ethanol.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-3a3934d1e4954577938127ae68982292
来源数据集: uspto-grants-2011_09
DOI: 10.6084/m9.figshare.5104873.v1
专利: US08017809B2
来源说明: uspto-grants-2011_09

反应 SMILES

[C:1]1([B:7]([CH:9]([O:16][CH:17]([B:24]([C:26]2[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=2)[OH:25])[C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)[C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)[OH:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[C:32]1([NH:38][CH2:39][CH2:40]O)[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=1>C(O)C>[C:1]1([B:7]([CH:9]([O:16][CH:17]([B:24]([C:26]2[CH:27]=[CH:28][CH:29]=[CH:30][CH:31]=2)[O:25][CH2:40][CH2:39][NH:38][C:32]2[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=2)[C:18]2[CH:19]=[CH:20][CH:21]=[CH:22][CH:23]=2)[C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)[O:8][CH2:40][CH2:39][NH:38][C:32]2[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=2)[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1