Nitric Acid → 6-Methoxy-5-nitro-1,2,3,4-tetrahydronaphthalen-1-one

HRID 1357870ノート

反応式

HRID 1357870 の反応式
[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[C:9](=[O:13])[CH2:8][CH2:7][CH2:6]2.S(=O)(=O)(O)O.[N+:19]([O-:22])([OH:21])=[O:20]>CC(C)=O>[CH3:1][O:2][C:3]1[C:4]([N+:19]([O-:21])=[O:20])=[C:5]2[C:10](=[CH:11][CH:12]=1)[C:9](=[O:13])[CH2:8][CH2:7][CH2:6]2.[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][C:12]=1[N+:19]([O-:22])=[O:20])[C:9](=[O:13])[CH2:8][CH2:7][CH2:6]2

参加物

6

反応条件

温度
0 °C

実験手順

To an ice-cold, stirred sloution of 6-methoxy-1-tetralone (17.6 g, 0.10 mol) in acetone (30 mL) was added dropwise a mixture of sulfuric acid (18 mL, 96.0%) and nitric acid (15 mL, 68.0-70.0%). After the addition was complete, the reaction was stirred at 0° C. for 6 hours, and TLC was employed to monitor the reaction progress. The reaction mixture was poured into ice-water, and the mixture was partitioned between CH2Cl2 (3*200 mL) and water (200 mL). The organic layer was washed by saturated NaHCO3 solution and water (200 mL each), dried over anhydrous sodium sulfate, and, after filtration, the organic layer was concentrated in vacuo to provide a yellow oil. 6-Methoxy-5-nitro-1-tetralone (7.74 g, 0.035 mol) and 6-methoxy-7-nitro-1-tetralone (6.63 g, 0.030 mol) was obtained after purification by column chromatography.

後処理

  1. additionwas added dropwise
  2. additionAfter the addition
  3. customthe mixture was partitioned between CH2Cl2 (3*200 mL) and water (200 mL)
  4. washThe organic layer was washed by saturated NaHCO3 solution and water (200 mL each)
  5. dry with materialdried over anhydrous sodium sulfate
  6. filtrationafter filtration
  7. concentrationthe organic layer was concentrated in vacuo
  8. customto provide a yellow oil

出典と根拠

ORDレコード
ord-08a49c84b1564e4e88040a767e1f03c2
出典データセット
uspto-grants-2003_07
特許番号
US06593374B2

反応ノート

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