3-Octadecyloxy-2-phthalimidopropan-1-ol → 1-Octadecyloxy-2-phthalimido-3-phenoxycarbonyloxypropane
Reaction equation
[CH2:1]([O:19][CH2:20][CH:21]([N:24]1[C:28](=[O:29])[C:27]2=[CH:30][CH:31]=[CH:32][CH:33]=[C:26]2[C:25]1=[O:34])[CH2:22][OH:23])[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].[CH2:35]([O:53][CH2:54]C(N)CO)[CH2:36][CH2:37][CH2:38][CH2:39][CH2:40]CCCCCCCCCCCC.C(C1C=CC=C2C(NC(=O)C=12)=O)(OCC)=[O:60]>>[CH2:1]([O:19][CH2:20][CH:21]([N:24]1[C:25](=[O:34])[C:26]2=[CH:33][CH:32]=[CH:31][CH:30]=[C:27]2[C:28]1=[O:29])[CH2:22][O:23][C:54]([O:53][C:35]1[CH:36]=[CH:37][CH:38]=[CH:39][CH:40]=1)=[O:60])[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
4
Procedure
3-Octadecyloxy-2-phthalimidopropan-1-ol used as the starting material was synthesized by reacting 3-octadecyloxy-2-aminopropane-1-ol as produced in Example 18-(i) with carboethoxyphthalimide.
Workup
- customwas synthesized
Sources & evidence
- ORD record
- ord-d9e46b532b7a4ef9acb310563494f7cb
- Source dataset
- uspto-grants-1991_06
- Patent number
- US05025005
Reaction notes
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