L-Malic Acid → HCID 14988496, compound
Reaction equation
[C:1]([OH:9])(=[O:8])[C@H:2]([CH2:4][C:5]([OH:7])=[O:6])[OH:3].F[C:11](F)(F)[C:12](O)=O.C1(=O)OC(=O)C[C@@H]1O>C(O)C>[CH2:11]([O:8][C:1](=[O:9])[C@H:2]([CH2:4][C:5]([OH:7])=[O:6])[OH:3])[CH3:12]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
By using the reagents, procedures and conditions described by Example 3A L-malic acid was converted to L-malic anhydride trifluoroacetate and the latter was allowed to react with ethyl alcohol to provide in 98.7% yield L-malic acid monoethyl ester melting at about 48° to about 49.5° C.
Sources & evidence
- ORD record
- ord-9a08ea084af546f385e19ea3e36dcd06
- Source dataset
- uspto-grants-1991_02
- Patent number
- US04992544
Reaction notes
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