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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 508064Generated: November 2, 2026

Trifluoroacetic acid → HCID 86624379, compound

https://huagongshe.com/reaction/508064

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 23157602HCID 23157602—
SolventTolueneHCID 1140—
SolventMethanesulfonic AcidHCID 6395—
SolventEthyl AcetateHCID 8857—
ProductHCID 86624379HCID 8662437980%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07786165B2
Source datasetuspto-grants-2010_08
ORD IDord-ba8228b2109f42c18b0ee2710f19222e
Source noteuspto-grants-2010_08