trans-2-Decenoic acid → 4-[(E)-2-Decenoyl]morpholine-3-carboxylic acid
Reaction equation
[C:1]([OH:12])(=[O:11])/[CH:2]=[CH:3]/[CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH3:10].Cl.[NH:14]1[CH2:19][CH2:18][O:17][CH2:16][CH:15]1[C:20]([O:22][CH3:23])=[O:21]>>[C:1]([N:14]1[CH2:19][CH2:18][O:17][CH2:16][CH:15]1[C:20]([O:22][CH3:23])=[O:21])(=[O:12])/[CH:2]=[CH:3]/[CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH3:10].[C:1]([N:14]1[CH2:19][CH2:18][O:17][CH2:16][CH:15]1[C:20]([OH:22])=[O:21])(=[O:11])/[CH:2]=[CH:3]/[CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH3:10]Participants
4
Procedure
The same procedures as in Example 2 were carried out using (E)-2-decenoic acid and methyl morpholine-3-carboxylate hydrochloride as starting raw materials, to produce methyl 4-[(E)-2-decenoyl)morpholine-3-carboxylate (methyl ester of Compound 49).
Sources & evidence
- ORD record
- ord-06a6cce71826434a9b9a7db82f3e2db9
- Source dataset
- uspto-grants-2016_08
- Patent number
- US09428477B2
Reaction notes
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