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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 328124Generated: October 26, 2026

Tetrahydrofuran → Nitraquazone

https://huagongshe.com/reaction/328124

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantEthyl chloroformateHCID 10928—
ReactantSodium hydrideHCID 24758—
Reactant2-(m-nitroanilino)-N-ethylbenzamideHCID 13305678—
SolventWaterHCID 962—
ProductNitraquazoneHCID 68765—

Reaction Steps

To a solution of 2.9 g of 2-(m-nitroanilino)-N-ethylbenzamide and 25 ml of tetrahydrofuran was added 1.0 g of 50 % sodium hydride, and stirring was performed for 30 minutes at room temperature. To this was added dropwise under cooling 5.4 g of ethyl chlorocarbonate, and the mixture was allowed to stand for one hour at room temperature and then refluxed for 10 hours. After the reaction was complete, the solvent was evaporated from the reaction mixture under reduced pressure, and to the residue obtained was added water to prepicpitate a crude product. This product was recrystallized from methanol to give 2.5 g of 1-(m-nitrophenyl)-3-ethylquinazoline-2,4(1H, 3H)-dione as colorless prisms, melting at 193°-194° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04016166
Source datasetuspto-grants-1977_04
ORD IDord-0cf5d302d5a14ad78d22f3d4b362dcfb
Source noteuspto-grants-1977_04