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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1830795Generated: October 31, 2026

Methanol → 5-Bromo-3-(3-chlorophenyl)-2,1-benzisoxazole

https://huagongshe.com/reaction/1830795

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant1-Bromo-4-nitrobenzeneHCID 11466—
ReactantSodium HydroxideHCID 14798—
Reactantm-ChlorophenylacetonitrileHCID 73722—
SolventWaterHCID 962—
Product5-Bromo-3-(3-chlorophenyl)-2,1-benzisoxazoleHCID 1201667034.8%

Reaction Steps

Sodium hydroxide (0.62 mol) was dissolved in methanol (100 mol) and the mixture was cooled till room temperature. 1-bromo-4-nitro-benzene (0.124 mol), followed by 3-chloro-benzeneacetonitrile (0.223 mol) were added dropwise, the temperature raised till 50° C. and the mixture was stirred at room temperature for one night. The mixture was poured into water and ice, the precipitate was filtered off, washed with water and extracted with DME and methanol. The organic layer was dried (MgSO4), filtered off and evaporated till dryness. The residue was taken up in diethylether, filtered off and dried, yielding 13.2 g (34.8%) of 5-bromo-3-(3-chlorophenyl)-2,1-benzisoxazole, mp. 163° C. (intermediate 1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07067531B2
Source datasetuspto-grants-2006_06
ORD IDord-d43f8168d14e4e5a9ea48f992ca7aae4
Source noteuspto-grants-2006_06