Pipecolic acid, (-)- → Pipecolic Acid
Reaction equation
[CH2:1]1[CH2:6][C@@H:5]([C:7]([OH:9])=[O:8])[NH:4][CH2:3][CH2:2]1>O>[NH:4]1[CH2:3][CH2:2][CH2:1][CH2:6][CH:5]1[C:7]([OH:9])=[O:8]Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
The filtrate is evaporated and dissolved in 5% acetic acid. Finally the solution is treated with Amberlite IR 45* in an ion exchanger. The eluate thus obtained is evaporated and the resulting crystalline residue is dried with potassium hydroxide in vacuo. The product obtained consists of L-pipecolic acid [α]24D -26.2°(C=5**, H2O).
Workup
- customThe filtrate is evaporated
- dissolutiondissolved in 5% acetic acid
- additionFinally the solution is treated with Amberlite IR 45* in an ion exchanger
- customThe eluate thus obtained
- customis evaporated
- dry with materialthe resulting crystalline residue is dried with potassium hydroxide in vacuo
- customThe product obtained
Sources & evidence
- ORD record
- ord-9084e86048ed490f8685a6aaecd86184
- Source dataset
- uspto-grants-1987_09
- Patent number
- US04695576
Reaction notes
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