Ethyl Acetate → HCID 21698569、化合物

HRID 379350ノート

反応式

HRID 379350 の反応式
[CH2:1]([C:3]1([CH3:24])[CH2:8][C:7]([CH3:10])([CH3:9])[CH2:6][CH:5]([NH:11][C:12](=[O:23])[C:13]2[CH:18]=[CH:17][CH:16]=[C:15]([N+:19]([O-])=O)[C:14]=2[OH:22])[CH2:4]1)[CH3:2].[H][H].[C:27](OCC)(=[O:29])C>[Pd]>[CH:27]([NH:19][C:15]1[C:14]([OH:22])=[C:13]([CH:18]=[CH:17][CH:16]=1)[C:12]([NH:11][CH:5]1[CH2:6][C:7]([CH3:10])([CH3:9])[CH2:8][C:3]([CH2:1][CH3:2])([CH3:24])[CH2:4]1)=[O:23])=[O:29]

参加物

5

実験手順

To a solution of N-(3-ethyl-3,5,5-trimethylcyclohexyl)-2-hydroxy-3-nitrobenzamide (3.60 g) in ethyl acetate (75 ml) was added 5% Pd/C (0.40 g) catalyst. The resulting mixture was subjected to a hydrogen atmosphere (initial H2 pressure=50 psi) using a Parr shaker apparatus. When hydrogen uptake ceased (approximately 30 minutes), the hydrogen atmosphere was purged. A stir bar was added to the reaction bottle and to the stirred reaction mixture acetic-formic anhydride (3 ml) was added all at once. After stirring at room temperature for 30 minutes, the reaction was filtered, washed with saturated sodium bicarbonate solution (100 ml). then with a saturated sodium chloride solution (100 ml), dried (MgSO4) and the solvent evaporated to give the desired product as a white solid foam (3.5 g). An analytical sample could be prepared by recrystallization from a methanol/water mixture to give an off-white crystalline solid (m.p.=166-168° C.). 13C NMR (CDCl3) showed this material to be approximately a 6:4 mixture of diastereomers.

後処理

  1. custom(approximately 30 minutes)
  2. customthe hydrogen atmosphere was purged
  3. additionA stir bar was added to the reaction bottle and to the stirred reaction mixture acetic-formic anhydride (3 ml)
  4. additionwas added all at once
  5. filtrationthe reaction was filtered
  6. washwashed with saturated sodium bicarbonate solution (100 ml)
  7. dry with materialthen with a saturated sodium chloride solution (100 ml), dried (MgSO4)
  8. customthe solvent evaporated

出典と根拠

ORDレコード
ord-81b8de6077244d4bbfa485f9dfc5e9ae
出典データセット
uspto-grants-2001_10
特許番号
US06297401B1

反応ノート

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