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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 898823Generated: October 30, 2026

4-(Trifluoromethyl)aniline → HCID 11301521, compound

https://huagongshe.com/reaction/898823

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Trifluoromethyl)anilineHCID 9964—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 5365845HCID 5365845—
SolventTolueneHCID 1140—
ProductHCID 11301521HCID 1130152175.3%

Reaction Steps

To a solution of 4-trifluoromethylaniline (193 mg, 1.2 mmol) and 3-crotonoyl-1,3-oxazolidin-2-one (155 mg, 1.0 mmol) in toluene (3 ml) in a stream of nitrogen was added Pd((R)-binap)(H2O)2(OTf)2 (26.6 mg, 0.025 mmol) and the resulting mixture was stirred at room temperature for 16 hours. After completion of the reaction, a saturated aqueous solution of ammonium chloride (10 ml) was added to the reaction mixture and the resulting mixture was extracted with ethyl acetate (10 ml). The organic layer was dried over anhydrous magnesium sulfate. The solvent was then evaporated off and the crude product obtained was purified by a silica gel column chromatography (hexane:ethyl acetate=1:1) to give the objective compound 3-(4-trifluoromethylanilino)butyryl-1,3-oxazolidin-2-one (238 mg, 75% yield). Enantiomeric excess ratio of this product was determined by a liquid chromatography using a column for separation of optical isomers (column: AD-H) to be 83% e.e.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07351849B2
Source datasetuspto-grants-2008_04
ORD IDord-c2539e421c084425899c51982ee7f755
Source noteuspto-grants-2008_04