Butyric Acid → Formate
Reaction equation
[C:1]([OH:5])(=[O:4])[CH2:2][OH:3].NCP(=O)(O)[OH:9].[C:12]([OH:17])(=[O:16])CCC.[C:18]([O-:22])(=[O:21])[CH2:19][OH:20]>>[C:1]([O-:5])(=[O:4])[CH:2]=[O:3].[CH:12]([O-:17])=[O:16].[C:19]([O-:9])(=[O:20])[C:18]([O-:22])=[O:21]Participants
7
Procedure
The reaction in Example 7 was repeated, using an aqueous solution containing glycolic acid (0.75M), aminomethylphosphonic acid (AMPA, 0.60M), FMN (0.01 mM), butyric acid (HPLC internal standard, 0.10M), glycolate oxidase (from spinach, 2.0 IU/mL), and catalase (from Aspergillus niger, 14,000 IU/mL) at pH 8.5.. After 40 h, the HPLC yields of glyoxylate, formate, and oxalate were 83.2%, 2.3%, and 7.5%, respectively, and no glycolate remained. The remaining activity of glycolate oxidase and catalase were 65% and 86%, respectively, of their initial values.
Workup
- customThe reaction in Example 7
Sources & evidence
- ORD record
- ord-0d16acaab32645f392b7fdd215a9b284
- Source dataset
- uspto-grants-1992_08
- Patent number
- US05135860
Reaction notes
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