2-Amino-3-hydroxyoctanoic acid → HCID 21416538, compound
Reaction equation
NC(C(O)CCCCC)C(O)=O.[C:13]([NH:16][CH:17]([CH:21]([OH:27])[CH2:22][CH2:23][CH2:24][CH2:25][CH3:26])[C:18](O)=[O:19])(=[O:15])[CH3:14].COC(=O)C(NC(=O)C)C(O)CCCCC.[H-].C([Al+]CC(C)C)C(C)C>CO>[C:13]([NH:16][CH:17]([CH:21]([OH:27])[CH2:22][CH2:23][CH2:24][CH2:25][CH3:26])[CH:18]=[O:19])(=[O:15])[CH3:14]Participants
6
Procedure
Protect the amino function in the 2-amino-3-hydroxyoctanoic acid by conversion thereof to an acetamido function, then esterify the resultant 2-acetamido-3-hydroxyoctanoic acid with methanol; reduce the resultant 2-acetamido-3-hydroxyoctanoic acid methyl ester with di-isobutylaluminum hydride according to known procedures to obtain 2-acetamido-3-hydroxyoctanal.
Sources & evidence
- ORD record
- ord-80bcba4fcc5940688da9bf420cede3fb
- Source dataset
- uspto-grants-1977_01
- Patent number
- US04002608
Reaction notes
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