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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2371010Generated: October 30, 2026

HCID 71184307, compound → (3R)-3-amino-4-(2,4,5-trifluorophenyl)butanoic Acid

https://huagongshe.com/reaction/2371010

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 71184307HCID 71184307—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product(3R)-3-amino-4-(2,4,5-trifluorophenyl)butanoic AcidHCID 714628393.2%

Reaction Steps

To a solution of 3 g (S)-methyl 3-(dibenzylamino)-4-oxo-4-(2,4,5-trifluorophenyl)butanoate in 100 ml ethanol, was added 0.5 g of 10% Pd/C under an atmosphere of nitrogen. The atmosphere of nitrogen was replace with an atmosphere of hydrogen, and the reaction was carried out at 25° C. for 5 h. After completion of the reaction, the reaction mixture was filtered through diatomite. The filtrate was concentrated, and the pH was adjusted to 5˜6 by addition of 10% hydrochloric acid. The aqueous layer was washed with ethyl acetate, and then concentrated to obtain 1.47 g (R)-3-amino-4-(2,4,5-trifluorophenyl)butanoic acid as white solid, with a yield of 93.2%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08710255B2
Source datasetuspto-grants-2014_04
ORD IDord-de50ab816e0c4d68989df5f69d129144
Source noteuspto-grants-2014_04