HRID1608906

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID18995395

未命名化合物

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

HCID20082763

未命名化合物

PRODUCTS

生成物

结构：CCCCOCC(F)(F)C(F)(F)C(F)(F)COc1ccc(OC(=O)c2ccc(OCCCC(C)CC)nc2)cc1

HCID20082762

未命名化合物

PROCEDURE

实验过程

4-(5-Butoxy-2,2,3,3,4,4-hexafluoropentoxy)phenyl 6-(4-methylhexyloxy)nicotinate (Compound 7, Table 1) was prepared by esterification of 4-(5-butoxy-2,2,3,3,4,4-hexafluoropentoxy)phenol (prepared essentially as in Example 5) with 6-(4-methylhexyloxy)nicotinic acid.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-572cebcbe3f442a8a5027aba939f12e7
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:24])([F:23])[C:8]([F:22])([F:21])[C:9]([F:20])([F:19])[CH2:10][O:11][C:12]1[CH:17]=[CH:16][C:15]([OH:18])=[CH:14][CH:13]=1)[CH2:2][CH2:3][CH3:4].[CH3:25][CH:26]([CH2:40][CH3:41])[CH2:27][CH2:28][CH2:29][O:30][C:31]1[CH:39]=[CH:38][C:34]([C:35](O)=[O:36])=[CH:33][N:32]=1>>[CH3:25][CH:26]([CH2:40][CH3:41])[CH2:27][CH2:28][CH2:29][O:30][C:31]1[CH:39]=[CH:38][C:34]([C:35]([O:18][C:15]2[CH:16]=[CH:17][C:12]([O:11][CH2:10][C:9]([F:19])([F:20])[C:8]([F:21])([F:22])[C:7]([F:23])([F:24])[CH2:6][O:5][CH2:1][CH2:2][CH2:3][CH3:4])=[CH:13][CH:14]=2)=[O:36])=[CH:33][N:32]=1