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Iodine chloride → 2-Fluoro-6-iodo-4-methylaniline

HRID 447751
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인쇄 미리보기

반응식

HRID 447751 반응식
[F:1][C:2]1[CH:8]=[C:7]([CH3:9])[CH:6]=[CH:5][C:3]=1[NH2:4].O.O.O.C([O-])(=O)C.[Na+].[I:18]Cl.C(=O)(O)[O-].[Na+].S([O-])([O-])=O.[Na+].[Na+]>C(O)(=O)C.C(OCC)C>[F:1][C:2]1[CH:8]=[C:7]([CH3:9])[CH:6]=[C:5]([I:18])[C:3]=1[NH2:4]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 24640Iodine chlorideHCID 679842-Fluoro-4-methylanilineHCID 18470521Sodium bicarbonate sodium sulfiteHCID 23665404Sodium Acetate Trihydrate

생성물 1

HCID 109779002-Fluoro-6-iodo-4-methylaniline

시약·촉매·용매 2

HCID 176Acetic Acid용매HCID 3283Diethyl Ether

실험 절차

A solution of 2-fluoro-4-methylaniline (1.0 g, 8 mmol) (bought from Avocado, Lancaster or Aldrich) in glacial acetic acid (10 ml) was treated with sodium acetate trihydrate (2.2 g, 16 mmol) then iodine monochloride (1.3 g). After 30 min at room temperature aqueous sodium bicarbonate/sodium sulfite and diethyl ether were added, and the organic phase was dried (MgSO4), evaporated and chromatographed on silica eluting with 0 to 30% ethyl acetate in hexane to give the title compound, 370 mg.

후처리

  1. dry with materialthe organic phase was dried (MgSO4)
  2. customevaporated
  3. customchromatographed on silica eluting with 0 to 30% ethyl acetate in hexane

출처 및 근거

ORD 기록
ord-1321d7bb5ab84781ba885aa67bff8733
출처 데이터셋
uspto-grants-2013_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08481566B2

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