Hydrogen Peroxide → 3-METHYLQUINOLINE N-OXIDE

HRID 2281115

反応式

HRID 2281115 の反応式
[CH3:1][C:2]1[CH:3]=[N:4][C:5]2[C:10]([CH:11]=1)=[CH:9][CH:8]=[CH:7][CH:6]=2.OO.[O-:14]S([O-])=O.[Na+].[Na+].[I-].[Na+].[OH-].[Na+]>C(O)(=O)C>[CH3:1][C:2]1[CH:3]=[N+:4]([O-:14])[C:5]2[C:10]([CH:11]=1)=[CH:9][CH:8]=[CH:7][CH:6]=2

参加物

7

反応条件

温度
80 °C

実験手順

3-Methylquinoline (30.0 mL, 224 mmol) was dissolved in acetic acid (85 mL), and 30% aqueous hydrogen peroxide (30.4 mL) was added. The reaction was stirred at 80° C. for 16 h before cooling in an ice bath. 10% aq Na2SO3 (199 mL, 0.5 equiv) was added followed by sodium iodide (2.358 g, 0.05 equiv). This mixture was stirred for 5 min. A peroxide test strip indicated no peroxide remaining. 5 N aq NaOH was then added, keeping the internal temperature below 24° C. A dark color formed, indicating that the solution was basic (tested as pH 10). The solution was extracted with four portions of dichloromethane. The combined organics were dried over MgSO4 and filtered, and the filtrate was concentrated under reduced pressure. Purification by silica gel flash chromatography (methanol/ethyl acetate) gave 3-methylquinoline 1-oxide (Intermediate 3, 32.09 g) as a yellow solid. 1H NMR (400 MHz, CDCl3) δ 8.69 (d, J=8.8 Hz, 1 H), 8.42 (s, 1 H), 7.77 (d, J=8.2 Hz, 1 H), 7.68 (td, J=7.8, 1.1 Hz, 1 H), 7.56-7.63 (m, 1 H), 7.52 (s, 1 H), 2.45 (s, 3 H); MS (M+1): 160.2.

後処理

  1. temperaturebefore cooling in an ice bath
  2. stirringThis mixture was stirred for 5 min
  3. customthe internal temperature below 24° C
  4. customA dark color formed
  5. extractionThe solution was extracted with four portions of dichloromethane
  6. dry with materialThe combined organics were dried over MgSO4
  7. filtrationfiltered
  8. concentrationthe filtrate was concentrated under reduced pressure
  9. customPurification by silica gel flash chromatography (methanol/ethyl acetate)

出典と根拠

ORDレコード
ord-6af6162a17d84757ae9e7db3b5b98af3
出典データセット
uspto-grants-2015_09
特許番号
US09139538B2

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