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Dimethylformamide → 4-Iodo-1-(2,2,2-trifluoroethyl)-1H-pyrazole

HRID 2205940
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HRID 2205940 반응식
[I:1][C:2]1[CH:3]=[N:4][NH:5][CH:6]=1.C(=O)([O-])[O-].[Cs+].[Cs+].CN(C=O)C.O([CH2:26][C:27]([F:30])([F:29])[F:28])S(C(F)(F)F)(=O)=O>O>[I:1][C:2]1[CH:3]=[N:4][N:5]([CH2:26][C:27]([F:30])([F:29])[F:28])[CH:6]=1
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참가 물질

6

반응물 4

HCID 6228DimethylformamideHCID 10796Cesium carbonateHCID 770224-IodopyrazoleHCID 803662,2,2-Trifluoroethyl trifluoromethanesulfonate

생성물 1

HCID 575166204-Iodo-1-(2,2,2-trifluoroethyl)-1H-pyrazole수율 103.5%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

A mixture of 4-iodo-pyrazole (582 mg, 3.0 mmole) and cesium carbonate (1.96 g, 6.0 mmole) was stirred with DMF (6 mL) for 5 minutes. Trifluoroethyl triflate (0.52 mL, 870 mg, 3.75 mmole) was added and the reaction was stirred at room temperature for 4.5 hours. The reaction was added to water (60 mL) and extracted with ether (3×25 mL). The combined organic extracts were washed with water (3×20 mL) and with brine; then dried (MgSO4) and evaporated to afford the title compound (857 mg, 89%). 1H-NMR (CDCl3, 500 MHz): δ 4.72 (q, J=8.20, 2H), 7.58 (s, 1H), 7.61 (s, 1H).

후처리

  1. extractionextracted with ether (3×25 mL)
  2. washThe combined organic extracts were washed with water (3×20 mL) and with brine
  3. dry with materialthen dried (MgSO4)
  4. customevaporated

출처 및 근거

ORD 기록
ord-81c614a2911741efb2701683913e2b0f
출처 데이터셋
uspto-grants-2016_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09371319B2

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