Picolinic acid → Isooctadecyl picolinate

HRID 1650122

Reaction equation

HRID 1650122 reaction equation
[N:1]1[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[C:7]([OH:9])=[O:8].[CH2:10](O)[CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH:25]([CH3:27])[CH3:26]>>[N:1]1[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[C:7]([O:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH:25]([CH3:26])[CH3:27])=[O:8]

Participants

3

Reactant 2

HCID 1018Picolinic acidHCID 62825Isostearyl Alcohol EX

Product 1

HCID 53805937Isooctadecyl picolinate

Procedure

Isooctadecyl picolinate was prepared using the method of Example 7 from picolinic acid and isooctadecyl alcohol, the commercial material obtained from Farbwerke Hoechst AG and described in Example 8. The light brown, oily product of the reaction had an estimated purity of 93.5%.

Sources & evidence

ORD record
ord-68f7731e7b774a75b83dc23275d87742
Source dataset
uspto-grants-1990_05
Patent number
US04923686

Linked notes

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