6-(4-Methylhexyloxy)nicotinic acid → 4-(5-Ethoxy-2,2,3,3,4,4-hexafluoropentoxy)phenyl 6-(4-methylhexyloxy)nicotinate

HRID 1608905Notes

Reaction equation

HRID 1608905 reaction equation
[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].[CH3:23][CH:24]([CH2:38][CH3:39])[CH2:25][CH2:26][CH2:27][O:28][C:29]1[CH:37]=[CH:36][C:32]([C:33](O)=[O:34])=[CH:31][N:30]=1>>[CH3:23][CH:24]([CH2:38][CH3:39])[CH2:25][CH2:26][CH2:27][O:28][C:29]1[CH:37]=[CH:36][C:32]([C:33]([O:16][C:13]2[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]=2)=[O:34])=[CH:31][N:30]=1

Participants

3

Procedure

4-(5-Ethoxy-2,2,3,3,4,4-hexafluoropentoxy)phenyl 6-(4-methylhexyloxy)nicotinate (Compound 6, 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 6-(4-methylhexyloxy)nicotinic acid.

Sources & evidence

ORD record
ord-a800e32cf3c8486baacc8b8a0e48ea05
Source dataset
uspto-grants-1995_03
Patent number
US05399291

Reaction notes

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