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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1772372Generated: November 2, 2026

Sodium Hydroxide → 1-(4-Bromo-3-methylisoxazol-5-yl)cyclopropane-1-carboxylic acid

https://huagongshe.com/reaction/1772372

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 1-(4-bromo-3-methylisoxazol-5-YL)cyclopropane-1-carboxylateHCID 67812454—
SolventTetrahydrofuranHCID 8028—
Product1-(4-Bromo-3-methylisoxazol-5-yl)cyclopropane-1-carboxylic acidHCID 6781257594.4%

Reaction Conditions

Temperature45 °C

Reaction Steps

To a solution of ethyl 1-(4-bromo-3-methylisoxazol-5-yl)cyclopropane-carboxylate (11.8 g, 43.0 mmol) in THF (60 mL) was added aqueous NaOH (86 mL, 86 mmol, 1 M). The dark brown bi-phasic reaction mixture was vigorously stirred and heated to 45° C. until consumption of SM (3-4 h) was detected by LC-MS and TLC analysis. After 4 h, the homogeneous mixture was cooled to room temperature and diluted with hexanes. The organic phase was separated and the aqueous phase (pH˜14) was acidified with aqueous 1 N HCl (pH 1) (˜100 mL). The product crystallizes upon acidification of the aqueous layer. After vigorously stirring for 30 min, the solids were filtered, washed with cold (0° C.) water (3×50 mL), and dried to give white crystals. The product 1-(4-bromo-3-methylisoxazol-5-yl)cyclopropanecarboxylic acid (10.0 g, 40.6 mmol, 94% yield) was isolated as white crystals. LC/MS m/z 246 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09249161B2
Source datasetuspto-grants-2016_02
ORD IDord-98b77d1b4044484b85678c29d52d0d2b
Source noteuspto-grants-2016_02