HRID1608907

反应详情

EQUATION

反应方程式

REACTANTS

反应物

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

HCID20082746

未命名化合物

HCID20082775

2-(Octyloxy)benzoic acid

C15H22O3

PRODUCTS

生成物

结构：CCCCCCCCOc1ccccc1C(=O)O.CCCCOCC(F)(F)C(F)(F)C(F)(F)COc1ccc2cc(O)ccc2c1

HCID86748560

未命名化合物

PROCEDURE

实验过程

6-(5-Butoxy-2,2,3,3,4,4-hexafluoropentoxy)-2-hydroxynapthalene octyloxybenzoate (Compound 8, Table 1) was prepared by esterification of 6-(5-butoxy-2,2,3,3,4,4-hexafluoropentoxy)-2-hydroxynapthalene (prepared essentially as in Example 8) with octyloxybenzoic acid.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-61a995b16bba485c843c36e3b6768728
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:5][CH2:6][C:7]([F:28])([F:27])[C:8]([F:26])([F:25])[C:9]([F:24])([F:23])[CH2:10][O:11][C:12]1[CH:13]=[C:14]2[C:19](=[CH:20][CH:21]=1)[CH:18]=[C:17]([OH:22])[CH:16]=[CH:15]2)[CH2:2][CH2:3][CH3:4].[CH2:29]([O:37][C:38]1[CH:46]=[CH:45][CH:44]=[CH:43][C:39]=1[C:40]([OH:42])=[O:41])[CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH3:36]>>[CH2:29]([O:37][C:38]1[CH:46]=[CH:45][CH:44]=[CH:43][C:39]=1[C:40]([OH:42])=[O:41])[CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH3:36].[CH2:1]([O:5][CH2:6][C:7]([F:27])([F:28])[C:8]([F:25])([F:26])[C:9]([F:23])([F:24])[CH2:10][O:11][C:12]1[CH:13]=[C:14]2[C:19](=[CH:20][CH:21]=1)[CH:18]=[C:17]([OH:22])[CH:16]=[CH:15]2)[CH2:2][CH2:3][CH3:4]