HRID1953928

反应详情

EQUATION

反应方程式

REACTANTS

反应物

结构：C[N+](C)(C)CCO.O=C([O-])c1ccccc1O.O=C([O-])c1ccccc1O.O=C([O-])c1ccccc1O.[Mg+2]

HCID178483604

未命名化合物

PRODUCTS

生成物

结构：O=C([O-])c1ccccc1O.O=C([O-])c1ccccc1O.[Mg+2]

HCID64738

Magnesium disalicylate

C14H10MgO6

HCID13035433

未命名化合物

HCID178483604

未命名化合物

HCID178524311

未命名化合物

AUXILIARIES

试剂、催化剂与溶剂

溶剂HCID962

Water

H2O

PROCEDURE

实验过程

A 10% solution of anionic salicylate was prepared by dissolving 10 g of choline magnesium trisalicylate (Trilisate™, Purdue Frederick, Norwalk, Conn.) in 87 g of distilled water. The mixture was stirred until the choline magnesium trisalicylate was fully dissolved. Each gram of choline magnesium trisalicylate yielded 587 mg of choline salicylate, 725 mg of magnesium salicylate being equivalent to 1 gram of salicylate content. Final composition:

WORKUP

后处理

dissolutionwas fully dissolved

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-7225513ac9304a5285794a41bdd68eda
来源数据集: uspto-grants-2000_09
DOI: 10.6084/m9.figshare.5104873.v1
专利: US06120756

反应 SMILES

[C:1]([O-:10])(=[O:9])[C:2]1[C:3](=[CH:5][CH:6]=[CH:7][CH:8]=1)[OH:4].[C:11]([O-:20])(=[O:19])[C:12]1[C:13](=[CH:15][CH:16]=[CH:17][CH:18]=1)[OH:14].[C:21]([O-:30])(=[O:29])[C:22]1[C:23](=[CH:25][CH:26]=[CH:27][CH:28]=1)[OH:24].[Mg+2:31].[OH:32][CH2:33][CH2:34][N+:35]([CH3:38])([CH3:37])[CH3:36]>O>[C:1]([O-:10])(=[O:9])[C:2]1[C:3](=[CH:5][CH:6]=[CH:7][CH:8]=1)[OH:4].[C:11]([O-:20])(=[O:19])[C:12]1[C:13](=[CH:15][CH:16]=[CH:17][CH:18]=1)[OH:14].[C:21]([O-:30])(=[O:29])[C:22]1[C:23](=[CH:25][CH:26]=[CH:27][CH:28]=1)[OH:24].[Mg+2:31].[OH:32][CH2:33][CH2:34][N+:35]([CH3:38])([CH3:37])[CH3:36].[C:1]([O:10][CH2:17][CH2:18][N+:35]([CH3:37])([CH3:36])[CH3:34])(=[O:9])[C:2]1[C:3](=[CH:5][CH:6]=[CH:7][CH:8]=1)[OH:4].[C:1]([O-:10])(=[O:9])[C:2]1[C:3](=[CH:5][CH:6]=[CH:7][CH:8]=1)[OH:4].[Mg+2:31].[C:1]([O-:10])(=[O:9])[C:2]1[C:3](=[CH:5][CH:6]=[CH:7][CH:8]=1)[OH:4].[C:1]([O-:10])(=[O:9])[C:2]1[C:3](=[CH:5][CH:6]=[CH:7][CH:8]=1)[OH:4]