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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1817790생성일: 2026년 10월 24일

Acetyl nitrate → 5-Nitrouracil

https://huagongshe.com/ko/reaction/1817790

반응식

참여 물질

역할이름HCID투입량
반응물Acetyl nitrateHCID 11557—
반응물Ethyl NitrateHCID 12259—
반응물Nitrous AcidHCID 24529—
반응물2,4(1H,3H)-Pyrimidinedione, amino-HCID 148782—
반응물Sodium NitriteHCID 23668193—
반응물Sulfuric acid, mixt. with nitric acidHCID 71777668—
반응물NaNO2 acetic acidHCID 86611488—
반응물3-nitroso-1H-pyrimidine-2,4-dioneHCID 86611489—
용매Acetic AcidHCID 176—
용매WaterHCID 962—
생성물5-NitrouracilHCID 69135—
생성물5-NitrosouracilHCID 328363—

반응 단계

The 5-nitrosouracil derivatives such as compound of the formula 4 may be obtained by the nitrosylation of the aminouracil 2 using standard nitration reagents. Examples of such agents include, for example, NaNO2/AcOH, HNO3/H2SO4, N2O5/P2O5/CCl4, HONO, EtONO2, CH3COONO2 and NO2+CF3SO3− that forms the nitro or the nitrosouracil derivative. Thus, the aminouracil 2 may be dissolved in an aqueous acid, such as acetic acid and water below room temperature, such as about 10° C., and NaNO2 in water is added to the aminouracil. When the reaction is deemed complete, the volatiles are removed under reduced pressure and the residue is redissolved in a mixture of solvents. Example of such mixtures of solvents include alcohols in an organic solvent, such as absolute ethanol in DICHLOROMETHANE. The resulting mixture is heated and the hot mixture may be filtered through a filter aid such as Celite 545 to remove insoluble inorganic salts. The solvent or solvent mixtures may evaporated under reduced pressure to afford the desired 5-nitrouracil or 5-nitrosouracil such as compound 4.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07598379B2
출처 데이터셋uspto-grants-2009_10
ORD IDord-233bf0d5a0a94d0699bfbbc82bef1539
출처 메모uspto-grants-2009_10