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Methyl iodide → HCID 14993733、化合物

HRID 1032481
ノート
印刷プレビュー

反応式

HRID 1032481 の反応式
[CH2:1]([N:8]1[CH2:16][C:15]2[C:10](=[CH:11][C:12]([O:19][CH3:20])=[C:13]([O:17][CH3:18])[CH:14]=2)[CH2:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH3:21][I:22]>CC(C)=O>[I-:22].[CH2:1]([N+:8]1([CH3:21])[CH2:9][C:10]2[C:15](=[CH:14][C:13]([O:17][CH3:18])=[C:12]([O:19][CH3:20])[CH:11]=2)[CH2:16]1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1
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 149937372-Benzyl-5,6-dimethoxyisoindoline

生成物 1

HCID 14993733HCID 14993733、化合物収率 14.4%

試薬・触媒・溶媒 1

HCID 180Acetone溶媒

実験手順

500 mg (1.86 mmol) of N-benzyl-5,6-dimethoxyisoindoline was dissolved in 10 ml of acetone, and 316 mg (2.27 mmol) of methyl iodide was added thereto at room temperature. The mixture was left to stand for 6 hours. Then, the precipitated crystals were collected by filtration and washed with 10 ml of acetone to obtain 640 mg of the above identified compound. The filtrate was distilled off under reduced pressure, and the crystal residue was washed with 10 ml of ethyl acetate to obtain 110 mg of the secondary crystals. The total yield was 750 mg.

後処理

  1. customat room temperature
  2. waitThe mixture was left
  3. filtrationThen, the precipitated crystals were collected by filtration
  4. washwashed with 10 ml of acetone
  5. customto obtain 640 mg of the
  6. distillationThe filtrate was distilled off under reduced pressure
  7. washthe crystal residue was washed with 10 ml of ethyl acetate

出典と根拠

ORDレコード
ord-265aff61a496450982f6daf228589443
出典データセット
uspto-grants-1990_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04958029

反応ノート

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