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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 405823Generated: October 30, 2026

Water → 3-(4-methyl-3-nitrophenyl)-1,2,4-oxadiazol-5(4H)-one

https://huagongshe.com/reaction/405823

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDiisopropylethylamineHCID 81531—
ReactantTriphosgeneHCID 94429—
ReactantN'-hydroxy-4-methyl-3-nitrobenzimidamideHCID 73711052—
SolventTetrahydrofuranHCID 8028—
Product3-(4-methyl-3-nitrophenyl)-1,2,4-oxadiazol-5(4H)-oneHCID 136334039—

Reaction Steps

To a solution of (Z)—N′-hydroxy-4-methyl-3-nitrobenzimidamide (27) (30 g, 153.71 mmol, 1.00 equiv) and DIEA (39.7 g, 307.18 mmol, 2.00 equiv) in tetrahydrofuran (300 mL) was added dropwise to a solution of triphosgene (18.2 g) in tetrahydrofuran (50 mL). The reaction was stirred for 1 hour at room temperature then heated to reflux for an additional hour. The resulting solution was poured into 500 mL of water and extracted with 3×300 mL of ethyl acetate. The combined organic layers were washed with brine (3×200 mL), dried over anhydrous sodium sulfate, concentrated under vacuum, and purified by flash chromatography (DCM/MeOH=20:1) to afford of 3-(4-methyl-3-nitrophenyl)-1,2,4-oxadiazol-5(4H)-one as a pale yellow solid (106). MS m/z 222.1 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08754071B2
Source datasetuspto-grants-2014_06
ORD IDord-9d4bb5d8274f46bbbc253be5026e72ae
Source noteuspto-grants-2014_06