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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1772371Generated: November 1, 2026

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

https://huagongshe.com/reaction/1772371

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 numberUS09249161B2
Source datasetuspto-grants-2016_02
ORD IDord-ef3ad1ff22af4d288c40e55970208052
Source noteuspto-grants-2016_02