Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2401427Generated: October 30, 2026

Water → Ethyl 1-(4-bromo-3-methylisoxazol-5-YL)cyclopropane-1-carboxylate

https://huagongshe.com/reaction/2401427

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 67811851HCID 67811851—
SolventDimethylformamideHCID 6228—
ProductEthyl 1-(4-bromo-3-methylisoxazol-5-YL)cyclopropane-1-carboxylateHCID 6781245494%

Reaction Steps

To a solution of ethyl 1-(3-methylisoxazol-5-yl)cyclopropanecarboxylate (9.49 g, 48.6 mmol) in anhydrous DMF (50 mL) was added N-bromosuccinimide (10.31 g, 57.9 mmol). The reaction mixture was stirred at room temperature for 24 h. To the orange mixture was added water and the aqueous layer was extracted with MTBE (3×). The combined organic layers were washed with aqueous 10% sodium thiosulfate, water (2×) and dried to provide the product ethyl 1-(4-bromo-3-methylisoxazol-5-yl)cyclopropanecarboxylate (12.5 g, 45.6 mmol, 94% yield) as a light yellow oil. The product was used directly in the subsequent reaction without further purification. LC/MS m/z 274 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08796261B2
Source datasetuspto-grants-2014_08
ORD IDord-b36149b9077a4b9faa073851f64e1cbe
Source noteuspto-grants-2014_08