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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 328125생성일: 2026년 10월 26일

Tetrahydrofuran → 1(m-nitrophenyl)-3-allylquinazoline-2,4(1H, 3H)-dione

https://huagongshe.com/reaction/328125

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물Sodium hydrideHCID 24758—
반응물Phosgen tolueneHCID 19083224—
반응물2-(m-nitroanilino)-N-allylbenzamideHCID 21444004—
용매WaterHCID 962—
생성물1(m-nitrophenyl)-3-allylquinazoline-2,4(1H, 3H)-dioneHCID 13272344—

반응 단계

To a solution of 3.0 g of 2-(m-nitroanilino)-N-allylbenzamide and 25 ml of tetrahydrofuran was added 1.1 g of 50 % sodium hydride, and the whole was stirred for 30 minutes at room temperature. To this was added dropwise under cooling 16 g of 30 % phosgene-toluene solution, and the mixture was stirred for one hour at room temperature and then refluxed for 2 hours. After the reaction was finished, the solvent was distilled off from the resulting mixture, and to the residue obtained was added water to precipitate a crude product. This product was recrystallized from methanol to yield 2.8 g of 1-(m-nitrophenyl)-3-allylquinazoline-2,4(1H, 3H)-dione as colorless needles, melting at 164°-166° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04016166
출처 데이터셋uspto-grants-1977_04
ORD IDord-275e0f4243df42678651f6d289c93cb3
출처 메모uspto-grants-1977_04