HRID1608908

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID18964568

未命名化合物

结构：CCOCC(F)(F)C(F)(F)C(F)(F)COc1ccc2cc(O)ccc2c1

HCID20082745

未命名化合物

PRODUCTS

生成物

结构：CCCCCCCCCCOc1ccccc1C(=O)O.CCOCC(F)(F)C(F)(F)C(F)(F)COc1ccc2cc(O)ccc2c1

HCID86748561

未命名化合物

PROCEDURE

实验过程

6-(5-Ethoxy-2,2,3,3,4,4-hexafluoropentoxy)-2-hydroxynapthalene decyloxybenzoate (Compound 9, Table 1) was prepared by esterification of 6-(5-ethoxy-2,2,3,3,4,4-hexafluoropentoxy)-2-hydroxynapthalene (prepared essentially as in Example 7) with decyloxybenzoic acid.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-0cda872032204afc8d9cb11e2e41a2ca
来源数据集: uspto-grants-1995_03
DOI: 10.6084/m9.figshare.5104873.v1
专利: US05399291
来源说明: uspto-grants-1995_03

反应 SMILES

[CH2:1]([O:3][CH2:4][C:5]([F:26])([F:25])[C:6]([F:24])([F:23])[C:7]([F:22])([F:21])[CH2:8][O:9][C:10]1[CH:11]=[C:12]2[C:17](=[CH:18][CH:19]=1)[CH:16]=[C:15]([OH:20])[CH:14]=[CH:13]2)[CH3:2].[CH2:27]([O:37][C:38]1[CH:46]=[CH:45][CH:44]=[CH:43][C:39]=1[C:40]([OH:42])=[O:41])[CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH3:36]>>[CH2:27]([O:37][C:38]1[CH:46]=[CH:45][CH:44]=[CH:43][C:39]=1[C:40]([OH:42])=[O:41])[CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH3:36].[CH2:1]([O:3][CH2:4][C:5]([F:25])([F:26])[C:6]([F:23])([F:24])[C:7]([F:21])([F:22])[CH2:8][O:9][C:10]1[CH:11]=[C:12]2[C:17](=[CH:18][CH:19]=1)[CH:16]=[C:15]([OH:20])[CH:14]=[CH:13]2)[CH3:2]