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3-[4-(1h-Pyrazol-1-yl)phenyl]-2-propyn-1-ol → 3-[4-(1H-pyrazol-1-yl)phenyl]-2-propynal

HRID 2416451
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반응식

HRID 2416451 반응식
[N:1]1([C:6]2[CH:11]=[CH:10][C:9]([C:12]#[C:13][CH2:14][OH:15])=[CH:8][CH:7]=2)[CH:5]=[CH:4][CH:3]=[N:2]1>CC(C)=O.O=[Mn]=O>[N:1]1([C:6]2[CH:11]=[CH:10][C:9]([C:12]#[C:13][CH:14]=[O:15])=[CH:8][CH:7]=2)[CH:5]=[CH:4][CH:3]=[N:2]1
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참가 물질

4

반응물 1

HCID 226309253-[4-(1h-Pyrazol-1-yl)phenyl]-2-propyn-1-ol

생성물 1

HCID 226308103-[4-(1H-pyrazol-1-yl)phenyl]-2-propynal수율 27%

시약·촉매·용매 2

HCID 14801Manganese dioxide촉매HCID 180Acetone용매

실험 절차

A mixture of the compound from step A (0.71 g, 3.58 mmol) and MnO2 (3.10 g, 35.66 mmol) in acetone (40 mL) was heated to reflux for 3 h. The cooled reaction mixture was filtered through Celite and the filtrate was concentrated. Purification by chromatography (SiO2, 6:1 hexane/ethyl acetate) yielded 0.19 g (27%) of the title compound as an off-white solid. MS 197 (M+H)+.

후처리

  1. temperaturewas heated
  2. temperatureto reflux for 3 h
  3. customThe cooled reaction mixture
  4. filtrationwas filtered through Celite
  5. concentrationthe filtrate was concentrated
  6. customPurification by chromatography (SiO2, 6:1 hexane/ethyl acetate)

출처 및 근거

ORD 기록
ord-e86d5d11c86c4fb1b2b5701a97a123d5
출처 데이터셋
uspto-grants-2004_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06825170B2

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