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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1844513Generated: October 27, 2026

Trifluoroacetic acid → HCID 56952644, compound

https://huagongshe.com/reaction/1844513

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 86698879HCID 86698879—
SolventDichloromethaneHCID 6344—
ProductHCID 56952644HCID 5695264491.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of tert-butyl methyl{3-methyl-4-[(5-{[4-(trifluoromethyl)benzoyl]amino}pyridin-2-yl)oxy]phenyl}carbamate (0.60 g) in CH2Cl2 (1 mL) was added TFA (3.32 mL) in three portion at 0° C. After stirring at 0° C. for 30 min, the mixture was evaporated under reduced pressure and the residue was dissolved in AcOEt. Ice cold 2 M NaOH (10 mL) was added, the mixture was extracted with AcOEt. The organic layer was washed with water and saturated aqueous NaCl, dried over anhydrous Na2SO4, and concentrated under reduced pressure. After addition of Et2O (20 mL), the solution was stirred vigorously. The resulting precipitate was collected and the precipitate was recrystallized from Et2O/AcOEt/Hexane to afford the title compound (0.44 g) as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946437B2
Source datasetuspto-grants-2015_02
ORD IDord-eb6ba5a16f2b45f1abd2b6f869f586be
Source noteuspto-grants-2015_02