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Triethylamine → N-(2-iodophenyl)methanesulfonamide

HRID 985718
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HRID 985718 반응식
[CH3:1][S:2](Cl)(=[O:4])=[O:3].[I:6][C:7]1[CH:13]=[CH:12][CH:11]=[CH:10][C:8]=1[NH2:9].C(N(CC)CC)C>ClCCl>[I:6][C:7]1[CH:13]=[CH:12][CH:11]=[CH:10][C:8]=1[NH:9][S:2]([CH3:1])(=[O:4])=[O:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 119952-IodoanilineHCID 31297Methanesulfonyl chloride

생성물 1

HCID 780001N-(2-iodophenyl)methanesulfonamide수율 75.4%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

Methanesulfonyl chloride (4.4 mL, 57 mmol) was added to a 0° C. dichloromethane (200 mL) solution containing 2-iodoaniline (5.0 g, 23 mmol) and triethylamine (9.6 mL, 69 mmol). The resulting mixture was stirred for 90 minutes, washed with HCl (0.5 M). The organics were separated then dried over sodium sulfate and concentrated in vacuo. The residue was then treated with potassium hydroxide (2.0 M in 1:1 methanol:water, 75 mL) for 30 min. This material was then diluted with dichloromethane and washed with HCl (1.0 N, 300 mL). The organics were separated then dried over sodium sulfate and concentrated to provide the title compound (5.15 g) as a tan solid.

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후처리

  1. washwashed with HCl (0.5 M)
  2. customThe organics were separated
  3. dry with materialthen dried over sodium sulfate
  4. concentrationconcentrated in vacuo
  5. additionThe residue was then treated with potassium hydroxide (2.0 M in 1:1 methanol:water, 75 mL) for 30 min
  6. additionThis material was then diluted with dichloromethane
  7. washwashed with HCl (1.0 N, 300 mL)
  8. customThe organics were separated
  9. dry with materialthen dried over sodium sulfate
  10. concentrationconcentrated

출처 및 근거

ORD 기록
ord-6a22d669e1cf487c81ae823682ef95a2
출처 데이터셋
uspto-grants-2005_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06872834B2

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