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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 70865Generated: October 26, 2026

Trifluoroacetic acid → (R)-4-biphenyl-4-yl-3-(3-carboxy-propionylamino)-butyric acid ethyl ester

https://huagongshe.com/reaction/70865

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantSuccinic anhydrideHCID 7922—
Reactant(R)-ethyl 4-(biphenyl-4-yl)-3-(tert-butoxycarbonylamino)butanoateHCID 59607632—
SolventDichloromethaneHCID 6344—
Product(R)-4-biphenyl-4-yl-3-(3-carboxy-propionylamino)-butyric acid ethyl esterHCID 4982222350.2%

Reaction Steps

To a solution of (R)-4-biphenyl-4-yl-3-tert-butoxycarbonylamino-butyric acid ethyl ester (400 mg, 1.04 mmol) in DCM (10 mL) at room temperature is added TFA (2.009 mL, 26.1 mmol) and the mixture is stirred at room temperature for 1 hour. The mixture is concentrated under reduced pressure. To the obtained TFA salt in DCM (10 mL) at ice bath temperature is added succinic anhydride (125 mg, 1.25 mmol) and followed by TEA (0.363 mL, 2.61 mmol). The reaction is stirred at room temperature for 16 hours. The mixture is concentrated under reduced pressure. The obtained residue is purified by flash chromatography (silica gel, 2% to 5% EtOH/DCM) give (R)-4-biphenyl-4-yl-3-(3-carboxy-propionylamino)-butyric acid ethyl ester (200 mg). HPLC retention time=1.53 minutes (condition C); MS=384 (m+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822534B2
Source datasetuspto-grants-2014_09
ORD IDord-d1bb9c9294a7440fa0cfad366f1f6fab
Source noteuspto-grants-2014_09