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Acetic Acid → HCID 69281520, 화합물

HRID 1487665
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HRID 1487665 반응식
[Cl:1][C:2]1[N:6]([CH:7]2[CH2:12][CH2:11][O:10][CH2:9][CH2:8]2)[N:5]=[CH:4][C:3]=1[N+:13]([O-])=O.C(O)(=O)C>O.[Fe]>[Cl:1][C:2]1[N:6]([CH:7]2[CH2:8][CH2:9][O:10][CH2:11][CH2:12]2)[N:5]=[CH:4][C:3]=1[NH2:13]
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참가 물질

5

반응물 2

HCID 176Acetic AcidHCID 69093111HCID 69093111, 화합물

생성물 1

HCID 69281520HCID 69281520, 화합물수율 52%

시약·촉매·용매 2

HCID 23925Iron촉매HCID 962Water용매

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온도
90 °C

실험 절차

To a suspension of 5-chloro-4-nitro-1-(tetrahydro-2H-pyran-4-yl)-1H-pyrazole (1 equiv) and iron dust (3 equiv) in water (0.35 M) was added acetic acid (3.54 M). The mixture was heated to 90° C. for 1.5 h then cooled to room temperature. The reaction was quenched by addition of solid sodium bicarbonate and treated with ethyl acetate (0.06M) with continuous stirring. The mixture was filtered and the filter cake was rinsed with ethyl acetate. The combined filtrate was dried over sodium sulfate and concentrated under reduced pressure. The crude product was purified by silica gel chromatography (1.5% MeOH in DCM) to provide the desired product (52% yield) as a brown oil. MS (ESI) m/z 202.1 [M+H]+.

후처리

  1. temperaturethen cooled to room temperature
  2. customThe reaction was quenched by addition of solid sodium bicarbonate
  3. additiontreated with ethyl acetate (0.06M) with continuous stirring
  4. filtrationThe mixture was filtered
  5. washthe filter cake was rinsed with ethyl acetate
  6. dry with materialThe combined filtrate was dried over sodium sulfate
  7. concentrationconcentrated under reduced pressure
  8. customThe crude product was purified by silica gel chromatography (1.5% MeOH in DCM)

출처 및 근거

ORD 기록
ord-9191dd3a8f354ceaa70e8e0e9041a126
출처 데이터셋
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09428509B2

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