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Methyl iodide → HCID 14993733, 화합물

HRID 1032481
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HRID 1032481 반응식
[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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6328Methyl iodideHCID 149937372-Benzyl-5,6-dimethoxyisoindoline

생성물 1

HCID 14993733HCID 14993733, 화합물수율 14.4%

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-265aff61a496450982f6daf228589443
출처 데이터셋
uspto-grants-1990_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04958029

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