Hexachloroethane → HCID 86726475, 화합물

HRID 1487640노트

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HRID 1487640 반응식
[CH3:1][O:2][CH2:3][CH2:4][N:5]1[CH:9]=[C:8]([N+:10]([O-:12])=[O:11])[CH:7]=[N:6]1.C[Si]([N-][Si](C)(C)C)(C)C.[Li+].[Cl:23]C(Cl)(Cl)C(Cl)(Cl)Cl>C1COCC1.[Cl-].[Na+].O>[Cl:23][C:9]1[N:5]([CH2:4][CH2:3][O:2][CH3:1])[N:6]=[CH:7][C:8]=1[N+:10]([O-:12])=[O:11]

참가 물질

6

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온도
-78 °C

실험 절차

To a solution of 1-(2-methoxyethyl)-4-nitro-1H-pyrazole (1 equiv) in THF (0.5 M) was added dropwise lithium bis(trimethylsilyl)amide (2.7 equiv) in THF (1.0 M) at −78° C. The reaction was stirred at −78° C. for 30 min before the addition of hexachloroethane (1.5 equiv) in THF (1.84 M). The reaction was stirred at −78° C. for 2.5 h before warming to room temperature. The reaction was diluted with brine and extracted with ethyl acetate. The combined extracts were washed with brine, dried over sodium sulfate, filtered and concentrated. The crude product was purified by flash chromatography (10-20% ethyl acetate in petroleum ether) to afford the desired product as a yellow solid (83% yield). 1H NMR (400 MHz, CHLOROFORM-d1) δ ppm 8.13 (s, 1H), 8.08 (s, 1H), 4.31-4.28 (t, J=4.2 Hz, 2H), 3.74-3.72 (t, J=5.36 Hz, 2H), 3.37 (s, 3H).

후처리

  1. temperaturebefore warming to room temperature
  2. extractionextracted with ethyl acetate
  3. washThe combined extracts were washed with brine
  4. dry with materialdried over sodium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customThe crude product was purified by flash chromatography (10-20% ethyl acetate in petroleum ether)

출처 및 근거

ORD 기록
ord-cc30a75218794d8381c71416b9686241
출처 데이터셋
uspto-grants-2016_08
특허 번호
US09428509B2

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