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Dimethyl Sulfate → 1-Methyl-2-phenyl-3-oxo-4-(-3-trifluoromethylphenyl)-5-methylamino-4-pyrroline

HRID 236244
ノート
印刷プレビュー

反応式

HRID 236244 の反応式
[CH3:1][N:2]1[C:6]([NH2:7])=[C:5]([C:8]2[CH:13]=[CH:12][CH:11]=[C:10]([C:14]([F:17])([F:16])[F:15])[CH:9]=2)[C:4](=[O:18])[CH:3]1[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1.[OH-].[Na+].S(OC)(O[CH3:31])(=O)=O.C([N+](CC)(CC)CC)C1C=CC=CC=1>O.[Cl-].C([N+](CC)(CC)CC)C1C=CC=CC=1.C(Cl)Cl>[CH3:1][N:2]1[C:6]([NH:7][CH3:31])=[C:5]([C:8]2[CH:13]=[CH:12][CH:11]=[C:10]([C:14]([F:16])([F:17])[F:15])[CH:9]=2)[C:4](=[O:18])[CH:3]1[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 4

HCID 6497Dimethyl SulfateHCID 14798Sodium HydroxideHCID 17208BenzyltriethylammoniumHCID 178481250HCID 178481250、化合物

生成物 1

HCID 138523621-Methyl-2-phenyl-3-oxo-4-(-3-trifluoromethylphenyl)-5-methylamino-4-pyrroline

試薬・触媒・溶媒 3

HCID 66133
Benzyl triethylammonium chloride
触媒
HCID 962Water溶媒
HCID 6344Dichloromethane溶媒2 回

実験手順

In this example, 4.1 g of 1-methyl-2-phenyl-3-oxo-4-(3-trifluoromethylphenyl)-5-amino-4-pyrroline, was added to 100 ml of methylene chloride containing 1.0 g of sodium hydroxide, dissolved in 4.0 ml of water, and 0.28 g of benzyltriethylammonium chloride at room temperature. Dimethyl sulfate (1.17 ml) dissolved in 20 ml of methylene chloride was admixed dropwise to the aforementioned mixture at room temperature. After the addition was complete, another 0.28 g of benzyltriethylammonium was added and the mixture was stirred at room temperature for 18 hours. At the end of this time, a white precipitate was collected from the mixture by filtration. This solid was stirred with 50 ml of 1N aqueous hydrochloric acid for two hours after which it was collected with suction filtration and washed with aqueous sodium bicarbonate solution followed by water. The solid was dried affording 1.0 g of the title compound as a white powder.

後処理

  1. customat room temperature
  2. customwas admixed dropwise to the aforementioned mixture at room temperature
  3. additionAfter the addition
  4. filtrationAt the end of this time, a white precipitate was collected from the mixture by filtration
  5. stirringThis solid was stirred with 50 ml of 1N aqueous hydrochloric acid for two hours after which it
  6. filtrationwas collected with suction filtration
  7. washwashed with aqueous sodium bicarbonate solution
  8. customThe solid was dried

出典と根拠

ORDレコード
ord-b4fff504db6c46ceb43b9b6088bb0deb
出典データセット
uspto-grants-1987_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04643762

反応ノート

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