Picolinic acid → Isooctadecyl picolinate

HRID 2119212

Reaction equation

HRID 2119212 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 Fabwerke 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-f6f2c00ce1454ad097bfed90eba8c035
Source dataset
uspto-grants-1987_07
Patent number
US04683310

Linked notes

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