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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1880699Generated: November 2, 2026

Sodium hydride → HCID 59570395, compound

https://huagongshe.com/reaction/1880699

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 59570398HCID 59570398—
ReactantHCID 178517507HCID 178517507—
SolventDimethylformamideHCID 6228—
ProductHCID 59570395HCID 5957039555%

Reaction Steps

Into 2 ml of N,N-dimethylformamide was suspended 0.07 g of sodium hydride (60% oily), and 0.3 g of 3-(4-trifluoromethylpyridin-2-yl)-1,2,4-oxadiazol-5-one was added at room temperature. After stirring for 15 minutes, 0.37 g of chloromethyl 3,5-dichlorobenzoate was added, and the mixture was stirred at 70° C. for 4 hours. The reaction solution was allowed to cool to room temperature, and poured into an aqueous saturated ammonium chloride solution, followed by extraction with ethyl acetate three times. The organic layers were combined, washed with an aqueous saturated sodium chloride solution, dried with anhydrous magnesium sulfate, and concentrated. The residue was subjected to silica gel column chromatography to obtain 0.31 g of [3-(4-trifluoromethylpyridin-2-yl)-1,2,4-oxadiazol-5-on-4-yl]methyl 3,5-dichlorobenzoate (present compound (39)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318776B2
Source datasetuspto-grants-2012_11
ORD IDord-47f44cb5105d4b62ab3fd40ac5f44ca0
Source noteuspto-grants-2012_11