HRID1608903

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID77412

Phenol, 4-(octyloxy)-

C14H22O2

结构：CCCCOCC(F)(F)C(F)(F)C(F)(F)COc1ccc(C(=O)O)cc1

HCID20082756

未命名化合物

PRODUCTS

生成物

结构：CCCCCCCCOc1ccc(OC(=O)c2ccc(OCC(F)(F)C(F)(F)C(F)(F)COCCCC)cc2)cc1

HCID20082742

未命名化合物

PROCEDURE

实验过程

4-Octyloxyphenyl 4-(5-butoxy-2,2,3,3,4,4-hexafluoropentoxy)benzoate (Compound 4, Table 1) was prepared by esterification of 4-(5-butoxy-2,2,3,3,4,4-hexafluoropentoxy)benzoic acid (prepared essentially as in Example 9) with 4-octyloxyphenol .

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-fc6710729bda484eb2b77b501125518d
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:26])([F:25])[C:8]([F:24])([F:23])[C:9]([F:22])([F:21])[CH2:10][O:11][C:12]1[CH:20]=[CH:19][C:15]([C:16]([OH:18])=[O:17])=[CH:14][CH:13]=1)[CH2:2][CH2:3][CH3:4].[CH2:27]([O:35][C:36]1[CH:41]=[CH:40][C:39](O)=[CH:38][CH:37]=1)[CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH3:34]>>[CH2:1]([O:5][CH2:6][C:7]([F:25])([F:26])[C:8]([F:23])([F:24])[C:9]([F:21])([F:22])[CH2:10][O:11][C:12]1[CH:20]=[CH:19][C:15]([C:16]([O:18][C:39]2[CH:40]=[CH:41][C:36]([O:35][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH3:34])=[CH:37][CH:38]=2)=[O:17])=[CH:14][CH:13]=1)[CH2:2][CH2:3][CH3:4]