Diiodomethane → 2-Iodo-5-(trifluoromethyl)benzonitrile

HRID 505266

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HRID 505266 반응식
N[C:2]1[CH:9]=[CH:8][C:7]([C:10]([F:13])([F:12])[F:11])=[CH:6][C:3]=1[C:4]#[N:5].[I:14]CI.N(OC(C)(C)C)=O>C(#N)C.CCOCC>[I:14][C:2]1[CH:9]=[CH:8][C:7]([C:10]([F:13])([F:12])[F:11])=[CH:6][C:3]=1[C:4]#[N:5]

참가 물질

6

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온도
35 °C

실험 절차

To a solution of 2-amino-5-(trifluoromethyl)benzonitrile (15.1 g) and diiodomethane (24 mL) in acetonitrile (150 mL) at 35° C. was added t-butyl nitrite (21 mL) dropwise. The reaction was maintained at approximately 35° C. during the addition. The reaction was aged for 30 min and then heated to 60° C. for 30 minutes. The reaction mixture was cooled, diluted with ether and washed twice with water, twice with aqueous sodium bisulfite, water and then brine. The solution was dried over anhydrous MgSO4, filtered through a silica gel plug and then concentrated giving afford a red oil. The product was purified by silica gel chromatography eluting sequentially with hexanes, 3:1 hexanes/CH2Cl2 and 1:1 hexanes/CH2Cl2 to afford 2-iodo-5-(trifluoromethyl)benzonitrile. 1H NMR (CDCl3, 500 MHz) δ 8.10 (d, J=8.5 Hz, 1H), 7.85 (d, J=1.8 Hz, 1H), 7.52 (dd, J=8.5, 1.8 Hz, 1H).

후처리

  1. temperatureheated to 60° C. for 30 minutes
  2. temperatureThe reaction mixture was cooled
  3. washwashed twice with water, twice with aqueous sodium bisulfite, water
  4. dry with materialThe solution was dried over anhydrous MgSO4
  5. filtrationfiltered through a silica gel plug
  6. concentrationconcentrated
  7. customgiving
  8. customafford a red oil
  9. customThe product was purified by silica gel chromatography
  10. washeluting sequentially with hexanes, 3:1 hexanes/CH2Cl2 and 1:1 hexanes/CH2Cl2

출처 및 근거

ORD 기록
ord-fb8d127661f048279424961b47018219
출처 데이터셋
uspto-grants-2010_08
특허 번호
US07781426B2

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