홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Sodium methanesulfonate → HCID 22747447, 화합물

HRID 2246314
노트
인쇄 미리보기

반응식

HRID 2246314 반응식
[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4](I)[C:3]=1[F:9].[CH3:10][S:11]([O-])(=[O:13])=[O:12].[Na+]>CN(C)C(=O)C.[Cu](I)I>[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([S:11]([CH3:10])(=[O:13])=[O:12])[C:3]=1[F:9]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 638112Sodium methanesulfonateHCID 190666581,2-Difluoro-3-iodobenzene

생성물 1

HCID 22747447HCID 22747447, 화합물수율 72.5%

시약·촉매·용매 2

HCID 83717Copper iodide촉매HCID 31374Dimethylacetamide용매

실험 절차

1,2-Difluoro-3-iodobenzene (1.70 g; 7.08 mmol), 2.17 g (21.2 mmol) of sodium methanesulfonate and 4.03 g (21.2 mmol) of copper iodide were heated with stirring at 111° C. for 20 hours in 50 ml of N,N-dimethylacetamide. The reaction solution was filtered, chloroform was added to the filtrate and the mixture was washed with a saturated aqueous solution of sodium hydrogen carbonate. The organic layer was dried and concentrated and the resulting residue was purified by a silica gel column chromatography (hexane:ethyl acetate=2:1) to give 987 mg (yield: 72%) of 1,2-difluoro-3-methanesulfonylbenzene as a colorless transparent solution.

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트

후처리

  1. filtrationThe reaction solution was filtered
  2. additionchloroform was added to the filtrate
  3. washthe mixture was washed with a saturated aqueous solution of sodium hydrogen carbonate
  4. customThe organic layer was dried
  5. concentrationconcentrated
  6. customthe resulting residue was purified by a silica gel column chromatography (hexane:ethyl acetate=2:1)

출처 및 근거

ORD 기록
ord-5ebaa3e9af374c4c97da47c985b54541
출처 데이터셋
uspto-grants-2010_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07687502B2

반응 노트

불러오는 중…