Reaction equation
[CH2:1]([N:3]([CH2:5][CH3:6])[OH:4])[CH3:2].[CH2:7]([O:25][C:26](=[O:29])[CH:27]=[CH2:28])[CH2:8][CH2:9][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][CH3:24].CC(C)([O-])C.[K+]>O1CCCC1>[CH2:7]([O:25][C:26](=[O:29])[CH2:27][CH2:28][O:4][N:3]([CH2:5][CH3:6])[CH2:1][CH3:2])[CH2:8][CH2:9][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][CH3:24]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
The procedure of Example I is repeated using 4.46 g of N,N-diethylhydroxylamine, 16.03 g of n-octadecylacrylate and 0.56 g of potassium-tert-butoxide in 100 ml of tetrahydrofuran, to afford the title compound as a colorless liquid.
Sources & evidence
- ORD record
- ord-fc5a3342fe564b3fa23ee63fe449222b
- Source dataset
- uspto-grants-1987_05
- Patent number
- US04666962
Linked notes
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