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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 132602Generated: November 3, 2026

Hydrochloric Acid → 1-[3-(4-Bromophenyl)-5-methyl-4-isoxazolyl]ethanone

https://huagongshe.com/reaction/132602

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAcetylacetoneHCID 31261—
ReactantSodium ethoxideHCID 2723922—
Reactant4-Bromo-N-hydroxybenzene-1-carboximidoyl chlorideHCID 12440885—
SolventEthanolHCID 702—
Product1-[3-(4-Bromophenyl)-5-methyl-4-isoxazolyl]ethanoneHCID 2129615284%

Reaction Steps

Acetylacetone (1.25 mL, 12 mmol) was added to a sodium ethoxide solution 3.09 N (3.95 mL, 12 mmol) in EtOH (22 mL) at room temperature. The resulting yellow solution was cooled with a ice-bath and a cloudy solution of (E)- and/or (Z)-4-bromo-N-hydroxy-benzenecarboximidoyl chloride (2.35 g, 10 mmol) in EtOH (8 mL) was added dropwise within 10 min keeping the temperature below 5° C. The light yellow suspension was stirred at room temperature for 3 h and then acidified with 6 N HCl and then evaporated. The resulting mixture was extracted with ethyl acetate and the combined organic layers were then washed with water and brine, dried over Na2SO4 and evaporated. Purification by chromatography (SiO2, heptane:ethyl acetate:=100:0 to 7:3) afforded the title compound (2.35 g, 84%) as a light yellow oil. MS m/e: 280.1/282.1 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07388025B2
Source datasetuspto-grants-2008_06
ORD IDord-1048e235422045e7a2960d2eb01892ff
Source noteuspto-grants-2008_06