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Triethylamine → N-(2,5-dimethoxy-3,4,6-trimethylbenzyl)-N-methyl-2-(4-acetylamino-2-isopropyl-5-methylphenoxy)ethylamine

HRID 55387
ノート
印刷プレビュー

反応式

HRID 55387 の反応式
[CH3:1][NH:2][CH2:3][CH2:4][O:5][C:6]1[CH:11]=[C:10]([CH3:12])[C:9]([NH:13][C:14](=[O:16])[CH3:15])=[CH:8][C:7]=1[CH:17]([CH3:19])[CH3:18].[CH3:20][O:21][C:22]1[C:29]([CH3:30])=[C:28]([CH3:31])[C:27]([O:32][CH3:33])=[C:26]([CH3:34])[C:23]=1[CH2:24]Cl.C(N(CC)CC)C>CN(C)C=O>[CH3:20][O:21][C:22]1[C:29]([CH3:30])=[C:28]([CH3:31])[C:27]([O:32][CH3:33])=[C:26]([CH3:34])[C:23]=1[CH2:24][N:2]([CH2:3][CH2:4][O:5][C:6]1[CH:11]=[C:10]([CH3:12])[C:9]([NH:13][C:14](=[O:16])[CH3:15])=[CH:8][C:7]=1[CH:17]([CH3:19])[CH3:18])[CH3:1]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 8471TriethylamineHCID 108789291-(Chloromethyl)-2,5-dimethoxy-3,4,6-trimethylbenzeneHCID 19957678N-Methyl-2-(4-acetylamino-2-isopropyl-5-methylphenoxy)ethylamine

生成物 1

HCID 19957658N-(2,5-dimethoxy-3,4,6-trimethylbenzyl)-N-methyl-2-(4-acetylamino-2-isopropyl-5-methylphenoxy)ethylamine収率 75%

試薬・触媒・溶媒 1

HCID 6228
Dimethylformamide
溶媒

実験手順

N-Methyl-2-(4-acetylamino-2-isopropyl-5-methylphenoxy)ethylamine (4.94 g) and 2,5-dimethoxy-3,4,6-trimethylbenzyl chloride (4.29 g) were dissolved in N,N-dimethylformamide (70 ml), and triethylamine (1.89 g) was added dropwise while stirring the mixture at room temperature. The mixture was stirred at room temperature for 16.5 hours. After the reaction, the solvent was distilled off, and water was added. The mixture was extracted with ethyl acetate. The obtained organic layer was washed with saturated brine and dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The obtained crude product was purified by silica gel chromatography (eluent; ethyl acetate/benzene=1/1) to give 6.40 g of a pale-yellow solid. A portion (1.0 g) was taken therefrom and recrystallized from diisopropyl ether to give 0.62 g of the title compound (colorless crystals).

後処理

  1. stirringThe mixture was stirred at room temperature for 16.5 hours
  2. customAfter the reaction
  3. distillationthe solvent was distilled off
  4. additionwater was added
  5. extractionThe mixture was extracted with ethyl acetate
  6. washThe obtained organic layer was washed with saturated brine
  7. dry with materialdried over anhydrous sodium sulfate
  8. distillationthe solvent was distilled off under reduced pressure
  9. customThe obtained crude product
  10. customwas purified by silica gel chromatography (eluent; ethyl acetate/benzene=1/1)

出典と根拠

ORDレコード
ord-f9a8a70d8a224fc19a8a03acae303de4
出典データセット
uspto-grants-1997_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05624961

反応ノート

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