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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 903618생성일: 2026년 10월 26일

Nitric Acid → 3-(m-nitrophenyl)-5,8-dihydro-6,6,8-trimethyl-5,8-ethano-6H-pyrano[4,3-e]-as-triazine-4-oxide-monohydrate

https://huagongshe.com/reaction/903618

반응식

참여 물질

역할이름HCID투입량
반응물Nitric AcidHCID 944—
반응물Trifluoromethanesulfonic acidHCID 62406—
반응물Sodium BicarbonateHCID 516892—
반응물3-phenyl-5,8-dihydro-6,6,8-trimethyl-5,8-ethano-6H-pyrano [4,3-e]-as-triazine-4-oxideHCID 23337017—
용매DichloromethaneHCID 6344—
생성물3-(m-nitrophenyl)-5,8-dihydro-6,6,8-trimethyl-5,8-ethano-6H-pyrano[4,3-e]-as-triazine-4-oxide-monohydrateHCID 23337026—

반응 단계

To a mixture of 0.2 ml. (0.005 mole) fuming nitric acid and 1.5 g. (0.01 mole) trifluoromethanesulfonic acid in 15 ml. anhydrous methylene chloride maintained at a temperature of -30° C. there is added dropwise a solution of 0.60 g. (0.002 mole) 3-phenyl-5,8-dihydro-6,6,8-trimethyl-5,8-ethano-6H-pyrano[4,3-e]-as-triazine-4-oxide in 15 ml. methylene chloride, maintaining the temperature at -30° C. throughout the addition. The resulting mixture is allowed to stir at ambient temperature for 72 hours, then poured onto ice and neutralized with solid sodium bicarbonate. The organic layer is removed, washed with saturated brine solution, dried over magnesium sulfate and evaporated. Trituration of the resulting residue with ether gives 3-(m-nitrophenyl)-5,8-dihydro-6,6,8-trimethyl-5,8-ethano-6H-pyrano[4,3-e]-as-triazine-4-oxide-monohydrate; m.p. 150° (d).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04228280
출처 데이터셋uspto-grants-1980_10
ORD IDord-72ec76eb786049f3849d53a26b817876
출처 메모uspto-grants-1980_10