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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1880696Generated: October 31, 2026

Sodium hydride → HCID 59570301, compound

https://huagongshe.com/reaction/1880696

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 21548637HCID 21548637—
ReactantHCID 178517507HCID 178517507—
SolventDimethylformamideHCID 6228—
ProductHCID 59570301HCID 5957030142.1%

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, 0.35 g of chloromethyl 4-t-butylbenzoate 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 0.23 g of [3-(4-trifluoromethylpyridin-2-yl)-1,2,4-oxadiazol-5-on-4-yl]methyl 4-t-butylbenzoate (present compound 36)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318776B2
Source datasetuspto-grants-2012_11
ORD IDord-fa8bb3f9b90e4e55b478544ac221cc21
Source noteuspto-grants-2012_11