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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 977216Generated: October 31, 2026

Trifluoroacetic acid → Trifluoroacetate

https://huagongshe.com/reaction/977216

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 70098694HCID 70098694—
ProductTrifluoroacetateHCID 84468—
ProductHCID 70099942HCID 70099942—

Reaction Steps

0.25 g of tert-butyl (2R)-2-[3-(4-amidinophenyl)-2-oxo-5-oxazolidinylcarbonylamino)-3phenylpropionate [obtainable according to Example 12]is stirred in 10 ml of trifluoroacetic acid at room temperature until hydrolysis is complete. The reaction mixture is subsequently concentrated and the residue is washed repeatedly with toluene. Treatment with ethyl acetate gives (2R)-2-[3-(4-amidinophenyl)-2-oxo-5-oxazolidinylcarbonylamino]-3-phenylpropionic acid, trifluoroacetate, FAB (M+1): 397.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05614535
Source datasetuspto-grants-1997_03
ORD IDord-3e68cd002b9a4163bb148e5b9b72231b
Source noteuspto-grants-1997_03