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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1514694Generated: November 3, 2026

Sodium hydride → 6-[3-(4-Chloro-phenyl)-5-([E]-styryl)-isoxazol-4-ylmethoxy]-nicotinic acid methyl ester

https://huagongshe.com/reaction/1514694

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantMethyl 6-chloropyridine-3-carboxylateHCID 254249—
Reactant[3-(4-Chloro-phenyl)-5-([E]-styryl)-isoxazol-4-yl]-methanolHCID 66643814—
SolventTetrahydrofuranHCID 8028—
Product6-[3-(4-Chloro-phenyl)-5-([E]-styryl)-isoxazol-4-ylmethoxy]-nicotinic acid methyl esterHCID 6671814064%

Reaction Steps

To a suspension of sodium hydride (2.64 g, 60.5 mmol) in THF (100 mL) was added a solution of [3-(4-chloro-phenyl)-5-([E]-styryl)-isoxazol-4-yl]-methanol (17.2 g, 55.0 mmol) in THF (185 mL) at 0° C. The reaction mixture was stirred for 60 min at room temperature. A solution of methyl 6-chloronicotinate (10.6 g, 60.5 mmol) in THF (185 mL) was added at 0° C. The mixture was stirred at room temperature for 2 h and the product was extracted with ethyl acetate/aqueous ammonium chloride and ethyl acetate/brine. Chromatography (silica, ethyl acetate:heptane 2:8 to 7:3) afforded the title compound (15.6 g, 64%) as a white solid. MS: m/e (%)=446 (0.7, M+), 309 (47), 294 (28), 240 (26), 131 (100), 103 (51).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08222246B2
Source datasetuspto-grants-2012_07
ORD IDord-225e9477e241484880fd32e92206c768
Source noteuspto-grants-2012_07