3-Fluoro-4-n-octyloxybenzoic Acid → 3-Fluoro-4-(2-methylnonanoyl) phenyl-3-fluoro-4-octyloxy benzoic acid

HRID 2372260Notes

Reaction equation

HRID 2372260 reaction equation
[F:1][C:2]1[CH:3]=[C:4](O)[CH:5]=[CH:6][C:7]=1[C:8](=[O:18])[CH:9]([CH3:17])[CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH3:16].[F:20][C:21]1[CH:22]=[C:23]([CH:27]=[CH:28][C:29]=1[O:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][CH2:37][CH3:38])[C:24]([OH:26])=[O:25]>>[F:1][C:2]1[CH:3]=[C:4]([C:22]2[C:21]([F:20])=[C:29]([O:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][CH2:37][CH3:38])[CH:28]=[CH:27][C:23]=2[C:24]([OH:26])=[O:25])[CH:5]=[CH:6][C:7]=1[C:8](=[O:18])[CH:9]([CH3:17])[CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH3:16]

Participants

3

Procedure

The same procedure as in Example 20 was repeated, except that (+)-3-fluoro-4-(2-methylnonanoyl) phenol was used instead of (+)-3-fluoro-4-(2-methylnonanoyl) phenol in Example 20 and 3-fluoro-4-octyloxy benzoic acid was used instead of 3-fluoro-4-heptyloxybenzoic acid in Example 20, to obtain an objective compound having the aforementioned physical and chemical properties.

Workup

  1. customto obtain an objective compound

Sources & evidence

ORD record
ord-2e4fe41cdaa1487aaa3fbd5810fd29e0
Source dataset
uspto-grants-1992_03
Patent number
US05098602

Reaction notes

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