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Methyl iodide → Ammonium, trimethyl(4-phenylbutyl)-, iodide

HRID 2371528
ノート
印刷プレビュー

反応式

HRID 2371528 の反応式
[CH3:1][N:2]([CH2:4][CH2:5][CH2:6][CH2:7][C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)[CH3:3].[CH3:14][I:15]>CO>[I-:15].[CH3:1][N+:2]([CH2:4][CH2:5][CH2:6][CH2:7][C:8]1[CH:9]=[CH:10][CH:11]=[CH:12][CH:13]=1)([CH3:14])[CH3:3]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 6328Methyl iodideHCID 13546746N,N-dimethyl-4-phenylbutylamine

生成物 1

HCID 43505Ammonium, trimethyl(4-phenylbutyl)-, iodide

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

To a solution of 287 mg of N,N-dimethyl-4-phenylbutylamine in 3 ml of absolute methanol, 505 μl of methyl iodide was added at a room temperature with stirring, and the mixture was stirred at a room temperature for 6.5 hours. The reaction mixture was concentrated under a reduced pressure, and after adding ethyl acetate allowed to stand for formation of crystal. The crystal was filtered, washed with ethyl acetate, and dried under a reduced pressure to obtain 439 mg of the title compound as a colorless crystal.

後処理

  1. stirringthe mixture was stirred at a room temperature for 6.5 hours
  2. concentrationThe reaction mixture was concentrated under a reduced pressure
  3. additionafter adding ethyl acetate
  4. filtrationThe crystal was filtered
  5. washwashed with ethyl acetate
  6. customdried under a reduced pressure

出典と根拠

ORDレコード
ord-964d41e7070c4735a4c768d94607c276
出典データセット
uspto-grants-1992_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05093370

反応ノート

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