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

HRID 2205940
ノート
印刷プレビュー

反応式

HRID 2205940 の反応式
[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
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

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

生成物 1

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

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

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).

後処理

  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

出典と根拠

ORDレコード
ord-81c614a2911741efb2701683913e2b0f
出典データセット
uspto-grants-2016_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09371319B2

反応ノート

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