Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1666713Generated: October 25, 2026

Formate → (R)-2-Amino-5,5,5-trifluoropentanoic acid

https://huagongshe.com/reaction/1666713

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormateHCID 283—
ReactantDL-alanineHCID 602—
ReactantPyridoxal 5'-phosphateHCID 1051—
ReactantLactateHCID 91435—
ReactantPyruvateHCID 107735—
ReactantNadhHCID 439153—
ReactantSodium FormateHCID 2723810—
Reactant5,5,5-Trifluoro-2-oxopentanoic acidHCID 14278600—
SolventPotassium Phosphate, TribasicHCID 62657—
Product(R)-2-Amino-5,5,5-trifluoropentanoic acidHCID 7177181—

Reaction Steps

The yields were increased by adding auxiliary enzymes to reduce pyruvate to lactate. Lactate dehydrogenase requires NADH as a cofactor. The NADH was regenerated using formate dehydrogenase. A solution containing 5,5,5-trifluoro-2-oxopentanoic acid (100 mg, 0.588 mmoles), D,L-alanine (200 mg, 2.244 mmoles), 0.02 mM pyridoxal phosphate, sodium formate (68 mg, 1 mmole), NAD (331 mg, 5 μmoles) L-lactate dehydrogenase cloned from rabbit muscle (Biocatalytics LDH-103, 0.107 mg, 15 units), and formate dehydrogenase (0.5 mL, 15 units cloned from Pichia pastoris and expressed in Escherichia coli) in 0.1 M potassium phosphate buffer, pH 7.5, was incubated with R-transaminase AT-103 from Biocatalytics (5 mg, 44 units) or cloned R-transaminase from Bacillus thuringiensis SC 16569 (0.5 mL, 10 units) at 30° C. in a total volume of 5 mL in 15 mL tubes. Reaction yields of (R)-5,5,5-trifluoro-2-aminopentanoic acid of 94% and 91% were obtained with AT-103 and BMS transaminases, respectively. Ee was 100% in both cases.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08044077B2
Source datasetuspto-grants-2011_10
ORD IDord-eecca44b0ee541cc8f84207823d3efdc
Source noteuspto-grants-2011_10