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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 223103Generated: October 26, 2026

Trifluoroacetic acid → L-Phenylalanyl-L-alanine

https://huagongshe.com/reaction/223103

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant1-(1(S)-t-butoxycarbonylethyl)-3(S)-azido-4(R)-phenylazetidin-2-oneHCID 13035214—
CatalystPalladiumHCID 23938—
ProductTrifluoroacetic acidHCID 6422—
ProductL-Phenylalanyl-L-alanineHCID 548819694%

Reaction Steps

After 1-(1(S)-t-butoxycarbonylethyl)-3(S)-azido-4(R)-phenylazetidin-2-one (300 mg., 0.95 mmol) was stirred in trifluoroacetic acid (2 ml.) at room temperature for 15 hours, the solvent was removed by distillation under reduced pressure. The thus obtained oil (360 mg.) was hydrogenated in 25 ml. of ethanol at 50° C. for 15 hours under ambient pressure using a 10% Pd-C (300 mg.) as a catalyst to give trifluoroacetic acid salt of L-phenylalanyl-L-alanine (311 mg., yield: 94%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04352752
Source datasetuspto-grants-1982_10
ORD IDord-8446506b615d4f04850806817179a906
Source noteuspto-grants-1982_10