HRID1608904

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID18995369

未命名化合物

结构：CCOCC(F)(F)C(F)(F)C(F)(F)COc1ccc(O)cc1

HCID20082750

未命名化合物

PRODUCTS

生成物

结构：CCCCCCCCOc1ccc(C(=O)Oc2ccc(OCC(F)(F)C(F)(F)C(F)(F)COCC)cc2)cc1Cl

HCID20082768

未命名化合物

PROCEDURE

实验过程

4-(5-Ethoxy-2,2,3,3,4,4-hexafluoropentoxy)phenyl 3-chloro-4-octyloxybenzoate (Compound 5, Table 1) was prepared by esterification of 4-(5-ethoxy-2,2,3,3,4,4-hexafluoropentoxy)phenol (prepared essentially as in Example 4) with 3-chloro-4-octyloxybenzoic acid.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-2f3324613d9f401d87ea5f8929b4a24d
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:22])([F:21])[C:6]([F:20])([F:19])[C:7]([F:18])([F:17])[CH2:8][O:9][C:10]1[CH:15]=[CH:14][C:13]([OH:16])=[CH:12][CH:11]=1)[CH3:2].[Cl:23][C:24]1[CH:25]=[C:26]([CH:30]=[CH:31][C:32]=1[O:33][CH2:34][CH2:35][CH2:36][CH2:37][CH2:38][CH2:39][CH2:40][CH3:41])[C:27](O)=[O:28]>>[Cl:23][C:24]1[CH:25]=[C:26]([CH:30]=[CH:31][C:32]=1[O:33][CH2:34][CH2:35][CH2:36][CH2:37][CH2:38][CH2:39][CH2:40][CH3:41])[C:27]([O:16][C:13]1[CH:14]=[CH:15][C:10]([O:9][CH2:8][C:7]([F:17])([F:18])[C:6]([F:19])([F:20])[C:5]([F:21])([F:22])[CH2:4][O:3][CH2:1][CH3:2])=[CH:11][CH:12]=1)=[O:28]