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N-methyl-2-pyrrolidone → 1-Fluoro-2-iodo-3-nitrobenzene

HRID 1722452
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HRID 1722452 반응식
FC(F)(F)S(O[C:7]1[C:12]([N+:13]([O-:15])=[O:14])=[CH:11][CH:10]=[CH:9][C:8]=1[F:16])(=O)=O.[I-:19].[Li+].CN1CCCC1=O>O>[I:19][C:7]1[C:8]([F:16])=[CH:9][CH:10]=[CH:11][C:12]=1[N+:13]([O-:15])=[O:14]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 13387N-methyl-2-pyrrolidoneHCID 66321Lithium iodideHCID 200290852-Fluoro-6-nitrophenyl Trifluoromethanesulfonate

생성물 1

HCID 234335971-Fluoro-2-iodo-3-nitrobenzene수율 47%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

A mixture consisting of 2-fluoro-6-nitrophenyl trifluoromethanesulfonate (62.0 g, 0.215 mol), lithium iodide (60 g, 0.451 mol) and 1-methyl-2-pyrrolidinone (400 mL) was heated with stirring at 130°-132° C. (oil bath temperature) for 18 hours. Upon cooling it was poured into water (1200 mL) and extracted with diethyl ether. The combined extracts were washed with 1N NaOH, water and with brine. The solution was dried (MgSO4), filtered, and concentrated in vacuo to give 27.0 g of the title compound as a brown-colored solid title compound (m.p. 54°-57° C.).

후처리

  1. temperaturewas heated
  2. temperatureUpon cooling it
  3. extractionextracted with diethyl ether
  4. washThe combined extracts were washed with 1N NaOH, water and with brine
  5. dry with materialThe solution was dried (MgSO4)
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-f5c8892df57b4e93b632b6f9ba793781
출처 데이터셋
uspto-grants-1989_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04855445

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