Aluminium lithium hydride → 2-Amino-2-(1,2-dihydroxy-4-octadecenyl)-1,3-propanediol
Reaction equation
[NH2:1][C:2]([CH:8]([OH:27])[CH:9]([OH:26])[CH2:10][CH:11]=[CH:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH3:25])([CH2:6][OH:7])[C:3](O)=[O:4].[H-].[Al+3].[Li+].[H-].[H-].[H-]>O1CCCC1>[NH2:1][C:2]([CH:8]([OH:27])[CH:9]([OH:26])[CH2:10][CH:11]=[CH:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH3:25])([CH2:3][OH:4])[CH2:6][OH:7]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A lactone compound (978 mg) of 2-amino-3-hydroxy-2-(1,2-dihydroxy-4-octadecenyl)propionic acid and 403 mg of lithium aluminum hydride were reacted in 33 ml of dry tetrahydrofuran according to the method of Example 274 to give 222 mg of the subject compound.
Sources & evidence
- ORD record
- ord-2b7c9da5aabf4c02a4055671e0c0ede2
- Source dataset
- uspto-grants-1998_02
- Patent number
- US05719176
Reaction notes
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