HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 508064Generated: November 2, 2026
Trifluoroacetic acid → HCID 86624379, compound
https://huagongshe.com/reaction/508064
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 23157602 | HCID 23157602 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Methanesulfonic Acid | HCID 6395 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86624379 | HCID 86624379 | 80% |
Reaction Steps
To a solution of tert-butyl 3-{4-[({4′-[2-(ethylsulfonyl)ethoxy]-2′,6′-dimethylbiphenyl-3-yl}methyl)amino]-2-fluorophenyl}propanoate (1.17 g, 2.05 mmol) in toluene (20 mL) was added trifluoroacetic acid (20 mL) under stirring at 0° C., and the mixture was stirred at room temperature for 1.5 hr. The reaction mixture was concentrated under reduced pressure, the residue was neutralized with saturated aqueous sodium hydrogencarbonate, and extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=2/1-hexane/ethyl acetate=1/4) to give a colorless oil. The obtained oil was diluted with ethyl acetate, and methanesulfonic acid (0.12 mL) was added. The precipitated crystals were collected by filtration, washed and dried to give the title compound (1.00 g, yield 80%) as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07786165B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-ba8228b2109f42c18b0ee2710f19222e |
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| Source note | uspto-grants-2010_08 |
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