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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2167490Generated: October 30, 2026

Trifluoroacetic acid → HCID 50914132, compound

https://huagongshe.com/reaction/2167490

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 58119388HCID 58119388—
SolventEthyl orthoformateHCID 31214—
ProductHCID 50914132HCID 50914132—
ProductHCID 58119388HCID 58119388—

Reaction Conditions

Temperature130 °C

Reaction Steps

4-{5-[(4-chlorophenyl)thio]-2-phenyl-1,3-oxazol-4-yl}benzohydrazide from Step C (33 mg, 0.077 mmol) was dissolved in 5 mL triethylorthoformate. A catalytic amount of TFA was added and the reaction was heated at 130° C. for 2 h. The volatiles were removed and the residue was purified by reverse phase HPLC to afford 12 mg (36% over 4 steps) of the title compound 2-(4-{5-[(4-chlorophenyl)thio]-2-phenyl-1,3oxazol-4-yl}phenyl)-1,3,4-oxadiazole. LCMS: m/z 432.1 (M+H)+. 1H NMR (500 MHz, CDCl3: δ 8.55 (1H, s), 8.40 (2H, d), 8.19 (4H, br), 7.55 (3H, br), 7.30 (4H, br).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09045467B2
Source datasetuspto-grants-2015_06
ORD IDord-1c67cffcb16b4604ae20aff5ec03b918
Source noteuspto-grants-2015_06