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Sodium Iodide → methyl N-(2-iodoethyl)-3-carbomethoxypyrrole-2-acetate

HRID 224463
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HRID 224463 반응식
S(O[CH2:6][CH2:7][N:8]1[CH:12]=[CH:11][C:10]([C:13]([O:15][CH3:16])=[O:14])=[C:9]1[CH2:17][C:18]([O:20][CH3:21])=[O:19])(C)(=O)=O.[I-:22].[Na+]>C(#N)C>[I:22][CH2:6][CH2:7][N:8]1[CH:12]=[CH:11][C:10]([C:13]([O:15][CH3:16])=[O:14])=[C:9]1[CH2:17][C:18]([O:20][CH3:21])=[O:19]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 5238Sodium IodideHCID 12795003methyl N-(2-mesyloxyethyl)-3-carbomethoxypyrrole-2-acetate

생성물 1

HCID 12795009methyl N-(2-iodoethyl)-3-carbomethoxypyrrole-2-acetate수율 97.3%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

A solution of 785 mg of methyl N-(2-mesyloxyethyl)-3-carbomethoxypyrrole-2-acetate and 1.83 g of sodium iodide in 10 ml of acetonitrile is refluxed for 1 hour. The cooled reaction mixture is evaporated to dryness under reduced pressure and the residue is triturated with water. The insoluble material is separated by filtration and is air dried, thus obtaining 840 mg (97%) of methyl N-(2-iodoethyl)-3-carbomethoxypyrrole-2-acetate (VI, R=H), m.p. 137°-138° C.

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후처리

  1. customThe cooled reaction mixture
  2. customis evaporated to dryness under reduced pressure
  3. customthe residue is triturated with water
  4. customThe insoluble material is separated by filtration
  5. customdried

출처 및 근거

ORD 기록
ord-6182539114784b43bf875b3133e853f1
출처 데이터셋
uspto-grants-1980_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04232038

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