HRID909834

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID7902

Dimethylaminoethanol

C4H11NO

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

HCID67392963

未命名化合物

PRODUCTS

生成物

结构：CN(C)CCOB(c1ccccc1)C(OC(B(OCCN(C)C)c1ccccc1)c1ccccc1)c1ccccc1

HCID67392614

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 (45 mg) was obtained by allowing 41 mg of bis(3,3′-(phenylhydroxyboryl)benzyl) ether and 19 mg of dimethylaminoethanol to act in 1 mL of ethanol.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-4ceb66e8735f497a8c212fa062df46e6
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.[CH3:32][N:33]([CH2:35][CH2:36]O)[CH3:34]>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][CH2:36][CH2:35][N:33]([CH3:34])[CH3:32])[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][CH2:36][CH2:35][N:33]([CH3:34])[CH3:32])[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1