反応式
[N+:1]([O-:4])(O)=[O:2].FC(F)(F)S(O)(=O)=O.[C:13]1([C:19]2[N:20]=[N:21][C:22]3[C:29]4([CH3:32])[CH2:30][CH2:31][CH:26]([C:27]([CH3:34])([CH3:33])[O:28]4)[C:23]=3[N+:24]=2[O-:25])[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1.C(=O)(O)[O-].[Na+]>C(Cl)Cl>[OH2:2].[N+:1]([C:15]1[CH:14]=[C:13]([C:19]2[N:20]=[N:21][C:22]3[C:29]4([CH3:32])[CH2:30][CH2:31][CH:26]([C:27]([CH3:34])([CH3:33])[O:28]4)[C:23]=3[N+:24]=2[O-:25])[CH:18]=[CH:17][CH:16]=1)([O-:4])=[O:2]参加物
実験手順
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).
後処理
- additionTo a mixture of 0.2 ml
- additionthere is added dropwise a solution of 0.60 g
- additionthroughout the addition
- customThe organic layer is removed
- washwashed with saturated brine solution
- dry with materialdried over magnesium sulfate
- customevaporated
出典と根拠
- ORDレコード
- ord-72ec76eb786049f3849d53a26b817876
- 出典データセット
- uspto-grants-1980_10
- 特許番号
- US04228280
関連ノート
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