Tetrahydrofuran → 4-Amino-2-iodobenzonitrile

HRID 723698노트

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HRID 723698 반응식
[I:1][C:2]1[CH:9]=[C:8]([N+:10]([O-])=O)[CH:7]=[CH:6][C:3]=1[C:4]#[N:5].O1CCCC1.[Cl-].[NH4+]>[Fe].C(O)C>[NH2:10][C:8]1[CH:7]=[CH:6][C:3]([C:4]#[N:5])=[C:2]([I:1])[CH:9]=1

참가 물질

6

실험 절차

A mixture of compound 489B (4.60 g, 16.8 mmol), tetrahydrofuran (75 mL), ethanol (100 mL), ammonium chloride solution (1.51 g, 28.3 mmol, dissolved in 100 mL of water), and iron (325 mesh, 4.21 g, 75.4 mmol) was mechanically stirred. The reaction mixture was heated to reflux for 3 h or until all starting material was consumed. The reaction mixture was cooled, filtered through Celite and concentrated in vacuo. The resulting residue was dissolved in ethyl acetate (200 mL) and washed with 1N sodium hydroxide (2×150 mL), dried over sodium sulfate, filtered and concentrated in vacuo to yield 3.97 g (97%) of compound 489C as a dark solid. HPLC: 95% at 1.877 min (retention time) (YMC S5 ODS column, 4.6×50 mm, eluting with 10–90% aqueous methanol over 4 min containing 0.2% phosphoric acid, 4 mL/min, monitoring at 220 nm). MS (ES): m/z 245.13 [M+H]+.

후처리

  1. temperatureThe reaction mixture was heated
  2. temperatureto reflux for 3 h or until all starting material
  3. customwas consumed
  4. temperatureThe reaction mixture was cooled
  5. filtrationfiltered through Celite
  6. concentrationconcentrated in vacuo
  7. dissolutionThe resulting residue was dissolved in ethyl acetate (200 mL)
  8. washwashed with 1N sodium hydroxide (2×150 mL)
  9. dry with materialdried over sodium sulfate
  10. filtrationfiltered
  11. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-2f2692fe2aff4c90b4a03ca787893ff7
출처 데이터셋
uspto-grants-2006_11
특허 번호
US07141578B2

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