Picolinic acid → Isooctadecyl picolinate

HRID 1248566

Reaction equation

HRID 1248566 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-8398af48b7fc423293d482d6696b26f5
Source dataset
uspto-grants-1985_06
Patent number
US04525330

Linked notes

Loading…