Allyl bromide → HCID 19780676, compound
Reaction equation
[C:1]([O:20][CH:21]1[CH2:26][CH2:25][N:24]([OH:27])[CH2:23][CH2:22]1)(=[O:19])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18].C(=O)([O-])[O-].[K+].[K+].[CH2:34](Br)[CH:35]=[CH2:36]>C(O)C>[C:1]([O:20][CH:21]1[CH2:26][CH2:25][N:24]([O:27][CH2:36][CH:35]=[CH2:34])[CH2:23][CH2:22]1)(=[O:19])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Repeating the general procedure of Example 1 using 1-hydroxy-piperdin-4-yl stearate, potassium carbonate and allyl bromide in ethanol solvent yields the title compound.
Sources & evidence
- ORD record
- ord-ca13ab4840b349a6b437ea88f37c161c
- Source dataset
- uspto-grants-1993_02
- Patent number
- US05185448
Reaction notes
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