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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Nitric Acid | HCID 944 | — |
| 반응물 | Trifluoromethanesulfonic acid | HCID 62406 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | 3-phenyl-5,8-dihydro-6,6,8-trimethyl-5,8-ethano-6H-pyrano [4,3-e]-as-triazine-4-oxide | HCID 23337017 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 3-(m-nitrophenyl)-5,8-dihydro-6,6,8-trimethyl-5,8-ethano-6H-pyrano[4,3-e]-as-triazine-4-oxide-monohydrate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04228280 |
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| 출처 데이터셋 | uspto-grants-1980_10 |
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| ORD ID | ord-72ec76eb786049f3849d53a26b817876 |
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| 출처 메모 | uspto-grants-1980_10 |
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