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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 897879Generated: October 30, 2026

Potassium tert-butoxide → HCID 22346863, compound

https://huagongshe.com/reaction/897879

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 178526352HCID 178526352—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 22346863HCID 2234686367.3%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of N1-(4-bromophenyl)-2-fluoro-1-benzeneamidoxime (1.51 g, 0.00489 mol) in N-methylpyrrolidinone (25 mL), potassium tert-butoxide (0.54 g, 0.00513 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 purified by flash chromatography on silica using ethyl acetate/n-heptane (1:5) as mobile phase to yield N-benzo[d]isoxazol-3-yl-N-(4-bromophenyl)amine (0.95 g, 0.00329 mol) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06921763B2
Source datasetuspto-grants-2005_07
ORD IDord-d66cfd7f72c94b29ab158c95605bb755
Source noteuspto-grants-2005_07