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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1198152Generated: October 31, 2026

Trifluoroacetic acid → HCID 10402602, compound

https://huagongshe.com/reaction/1198152

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 10089718HCID 10089718—
ProductHCID 10402602HCID 1040260257%

Reaction Conditions

Temperature-10 °C

Reaction Steps

Trifluoroacetic acid (1.3 ml) is added dropwise at -10° C. to 0.23 g (0.643 mmoles) of tert-butyl (E)-5-[1-phenyl-2-(imidazol-1-yl)ethylidene]aminoxypentanoate. The mixture is stirred at -10° C. for 1 hour and 30 minutes. A cooled saturated sodium hydrogencarbonate solution is added to the reaction mixture at 0° C. till pH=7 and the mixture is extracted with ethyl acetate. The aqueous phase is cooled, acidified with acetic acid and extracted twice with ethyl acetate. The organic phase is dried and evaporated. The residue is taken up twice with toluene and evaporated under vacuum without heating, yielding 0.11 g (57%) of (E)-5-[1-phenyl-2-(imidazol-1-yl)ethylidene]aminoxypentanoic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05280033
Source datasetuspto-grants-1994_01
ORD IDord-f3757ea4676a4497bf070aeb8929d28f
Source noteuspto-grants-1994_01