Potassium Permanganate → 5-Methoxy-4-(4-methoxy-4-oxobutoxy)-2-nitrobenzoic acid

HRID 476396

反応式

HRID 476396 の反応式
[CH3:1][O:2][C:3](=[O:21])[CH2:4][CH2:5][CH2:6][O:7][C:8]1[CH:13]=[C:12]([N+:14]([O-:16])=[O:15])[C:11]([CH:17]=[O:18])=[CH:10][C:9]=1[O:19][CH3:20].[Mn]([O-])(=O)(=O)=[O:23].[K+]>CC(C)=O>[CH3:20][O:19][C:9]1[C:8]([O:7][CH2:6][CH2:5][CH2:4][C:3]([O:2][CH3:1])=[O:21])=[CH:13][C:12]([N+:14]([O-:16])=[O:15])=[C:11]([CH:10]=1)[C:17]([OH:23])=[O:18]

参加物

4

反応物 2

HCID 516875Potassium PermanganateHCID 11033807Butanoic acid, 4-(4-formyl-2-methoxy-5-nitrophenoxy)-, methyl ester

生成物 1

HCID 589159645-Methoxy-4-(4-methoxy-4-oxobutoxy)-2-nitrobenzoic acid収率 50%

試薬・触媒・溶媒 1

HCID 180Acetone溶媒

実験手順

The slightly wet nitroaldehyde 12 (80 g, wet) was dissolved in acetone (500 mL) in a 2 L flask fitted with a condenser and a mechanical stirrer. A hot solution of 10% potassium permanganate (50 g in 500 mL of water) was quickly added via a dropping funnel (in 5 to 10 minutes). Halfway through the addition the solution began to reflux violently and until the end of the addition. The solution was allowed to stir and cool down for an hour and was then filtered through celite and the brown residue was washed with 1 L of hot water. The filtrate was transferred in a large flask and a solution of sodium bisulfite (80 g in 500 mL 1N HCl) was added. The final volume was adjusted to 3 L by addition of water, and the pH was adjusted to 1 with conc. HCl. The product 42 precipitated and it was filtered and dried. 31 g (50% yield over 2 steps). The product was pure as proved by TLC (85/15/0.5 EtOAc/MeOH/Acetic acid). 1H NMR (CDCl3) δ 7.33 (1H, s), 7.19 (1H, s), 4.09 (2H, t, J=5.72 Hz), 3.91 (3H, s), 3.64 (3H, s), 2.50 (2H, t, J=6.98 Hz), 2.14 (2H, p, J=6.33 Hz); 13C NMR (DMSO-d6) δ 172.8, 166.0, 151.8, 149.1, 141.3, 121.2, 111.3, 107.8, 68.1, 56.4, 51.3, 29.7, 23.8; IR (golden gate) vmax 1736, 1701, 1602, 1535, 1415, 1275, 1220, 1054, 936, 879, 820, 655 cm−1; MS (ES−) m/z (relative intensity) 312.01 ([M−H]−, 100).

後処理

  1. customfitted with a condenser and a mechanical stirrer
  2. additionHalfway through the addition the solution
  3. temperatureto reflux violently and until the end of the addition
  4. temperaturecool down for an hour
  5. filtrationwas then filtered through celite
  6. washthe brown residue was washed with 1 L of hot water
  7. customThe filtrate was transferred in a large flask
  8. additiona solution of sodium bisulfite (80 g in 500 mL 1N HCl) was added
  9. additionThe final volume was adjusted to 3 L by addition of water
  10. customThe product 42 precipitated
  11. filtrationit was filtered
  12. customdried

出典と根拠

ORDレコード
ord-fb36528a784941ffa6e9a0b1b17a4c74
出典データセット
uspto-grants-2014_01
特許番号
US08637664B2

関連ノート

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