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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2056184Generated: November 3, 2026

Potassium tert-butoxide → HCID 22346862, compound

https://huagongshe.com/reaction/2056184

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 178526353HCID 178526353—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 22346862HCID 2234686281.9%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of N1-(4-bromophenyl)-2-fluoro-4-(trifluoromethyl)-1-benzeneamidoxime (2.25 g, 0.00598 mol) in N-methylpyrrolidinone (30 mL), potassium tert-butoxide (0.71 g, 0.00628 mol) was added and the resulting solution was heated at 100° C. under an atmosphere of nitrogen for 3 hours. The reaction mixture was cooled to ambient temperature, the solvent was removed under reduced pressure and the residue partitioned between saturated solution of sodium bicarbonate in water (50 mL) and ethyl acetate (50 mL). The organic phase was washed with brine, dried with magnesium sulfate and concentrated. The residue was suspended in cold n-heptane and the precipitate was collected by filtration and dried to yield N-(4-bromophenyl)-N-[6-(trifluoromethyl)benzo[d]isoxazol-3-yl]amine (1.75 g, 0.0049 mol) as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07332497B2
Source datasetuspto-grants-2008_02
ORD IDord-b757d60bd89c41788eac9e715c3798ea
Source noteuspto-grants-2008_02