HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 332862Generated: October 30, 2026
Ammonium trifluoroacetate → HCID 178487663, compound
https://huagongshe.com/reaction/332862
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium trifluoroacetate | HCID 2724268 | — |
| Reactant | (E)-2-(4-((2-(4-fluoro-2-methylphenyl)-6-methoxybenzo[b]thiophen-3-yl)oxy)styryl)-5-methyl-1,3,4-oxadiazole | HCID 86730645 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 178487663 | HCID 178487663 | 65.3% |
Reaction Steps
To a microwave vial, (E)-2-(4-((2-(4-fluoro-2-methylphenyl)-6-methoxybenzo[b]thiophen-3-yl)oxy)styryl)-5-methyl-1,3,4-oxadiazole (23 mg, 0.049 mmol) and ammonium trifluoroacetate (128 mg, 0.973 mmol) were suspended in toluene (2 mL). The reaction was heated for 18 h at 180° C. under microwave irradiation. The reaction mixture was concentrated and the crude product was purified by reverse phase HPLC (neutral condition, 0.1% TFA in 20-100% CH3CN/H2O) to afford (E)-3-(4-((2-(4-fluoro-2-methylphenyl)-6-methoxybenzo[b]thiophen-3-yl)oxy)styryl)-5-methyl-4H-1,2,4-triazole (15 mg, 0.032 mmol, 65% yield) as a white solid. LC/MS (m/z, MH+): 472.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08877801B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-dd69b75c3587447eb33bc9a920ba4625 |
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| Source note | uspto-grants-2014_11 |
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