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Potassium Carbonate → 4-Ethynyl-1-(2,2,2-trifluoroethyl)-1H-pyrazole

HRID 2205942
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HRID 2205942 반응식
[F:1][C:2]([F:16])([F:15])[CH2:3][N:4]1[CH:8]=[C:7]([C:9]#[C:10][Si](C)(C)C)[CH:6]=[N:5]1.C(=O)([O-])[O-].[K+].[K+]>CO>[C:9]([C:7]1[CH:6]=[N:5][N:4]([CH2:3][C:2]([F:15])([F:16])[F:1])[CH:8]=1)#[CH:10]
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참가 물질

4

반응물 2

HCID 11430Potassium CarbonateHCID 682905641-(2,2,2-Trifluoroethyl)-4-((trimethylsilyl)ethynyl)-1H-pyrazole

생성물 1

HCID 867063294-Ethynyl-1-(2,2,2-trifluoroethyl)-1H-pyrazole수율 53%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

1-(2,2,2-Trifluoroethyl)-4-((trimethylsilyl)ethynyl)-1H-pyrazole (Preparation 147, 1.19 g) was dissolved in methanol (7 ml) and potassium carbonate (30 mg) was added. The reaction was stirred at room temperature for 3.5 hours. The methanol was evaporated and the residue taken up in dichloromethane (20 ml) and filtered through a plug of silica eluting with DCM to afford the title compound (326 mg, 53%). 1H-NMR (CDCl3, 500 MHz): δ 3.06 (s, 1H), 4.70 (q, J=8.20 Hz, 2H), 7.69 (s, 1H), 7.70 (s, 1H). 19F-NMR (CDCl3, 470.385 MHz): −71.69

후처리

  1. customThe methanol was evaporated
  2. filtrationfiltered through a plug of silica eluting with DCM

출처 및 근거

ORD 기록
ord-fb6067dfeed74c31b6985cce5654ac31
출처 데이터셋
uspto-grants-2016_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09371319B2

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