2-Propoxypropanoic acid → HCID 22155752, compound
Reaction equation
[CH2:1]([C:10]1[CH:11]=[CH:12][C:13]([C:16]2[CH:21]=[CH:20][C:19]([O:22][CH2:23][C@@H:24]([OH:26])[CH3:25])=[CH:18][CH:17]=2)=[N:14][CH:15]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH3:9].[CH2:27]([O:30][CH:31]([CH3:35])[C:32](O)=[O:33])[CH2:28][CH3:29]>>[CH2:1]([C:10]1[CH:11]=[CH:12][C:13]([C:16]2[CH:21]=[CH:20][C:19]([O:22][CH2:23][CH:24]([O:26][C:32](=[O:33])[CH:31]([O:30][CH2:27][CH2:28][CH3:29])[CH3:35])[CH3:25])=[CH:18][CH:17]=2)=[N:14][CH:15]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH3:9]Participants
3
Procedure
(S)-5-nonyl-2-(4'-(2"-hydroxypropoxy)phenyl)pyridine (m.p. 77.6°-80.3° C.) was reacted with 2-propoxypropionic acid prepared in Example 3 in the same manner as in Example 3 to obtain 5-nonyl-2-(4'-(2"-(2"'-propoxypropionyloxy)-propoxy)phenyl)pyridine (m.p. 58.0° C.).
Sources & evidence
- ORD record
- ord-9219680046464ea9b15857c53c48531c
- Source dataset
- uspto-grants-1990_11
- Patent number
- US04973426
Reaction notes
Loading…