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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 508104Generated: October 29, 2026

Trifluoroacetic acid → HCID 59434151, compound

https://huagongshe.com/reaction/508104

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 59434148HCID 59434148—
SolventDichloromethaneHCID 6344—
ProductHCID 59434151HCID 5943415179.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of tert-butyl 3-{4-[({4′-[(1,1-dioxidotetrahydro-2H-thiopyran-4-yl)methoxy]-2′,6′-dimethylbiphenyl-3-yl}methyl)amino]-2-fluorophenyl}propanoate (0.08 g, 0.14 mmol) in methylene chloride (2 mL) was added trifluoroacetic acid (2 mL) under stirring at 0° C., and the mixture was stirred at room temperature for 2 hr. The reaction mixture was concentrated under reduced pressure, and the residue was neutralized with saturated aqueous sodium hydrogencarbonate, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was recrystallized from ethyl acetate-hexane to give the title compound (0.06 g, yield 78%) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07786165B2
Source datasetuspto-grants-2010_08
ORD IDord-7ed7a022f0d0436a83fea76cd1c52d5c
Source noteuspto-grants-2010_08