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3-(3-Pyridyl)-2-propyn-1-ol → 3-(3-Pyridinyl)-2-propynal

HRID 1008761
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반응식

HRID 1008761 반응식
[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]([C:7]#[C:8][CH2:9][OH:10])[CH:2]=1>C(Cl)Cl.O=[Mn]=O>[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]([C:7]#[C:8][CH:9]=[O:10])[CH:2]=1
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참가 물질

4

반응물 1

HCID 121814423-(3-Pyridyl)-2-propyn-1-ol

생성물 1

HCID 227351693-(3-Pyridinyl)-2-propynal수율 17.4%

시약·촉매·용매 2

HCID 14801Manganese dioxide촉매HCID 6344Dichloromethane용매

실험 절차

To a solution of 3-(3-pyridinyl)-2-propyn-1-ol (250 mg, 1.88 mmol, obtained as described in J. Org Chem. 1998, 63, 1109-1118) in anhydrous DCM (10 ml) under argon was added MnO2 (3.66 g, 42 mmol) portion wise over 1.5 h. The reaction mixture was stirred at rt for one additional hour. Then the reaction mixture was poured on the top of a column of silica gel and eluted with cHex/EtOAc (2:1 then 1:1) to give 43 mg (17%) of the title compound as a yellow powder. 1H NMR (CDCl3) δ: 9.46 (s, 1H), 8.85 (dd, J=2.1, 0.8 Hz, 1H), 8.71 (dd, J=5.0, 1.7 Hz, 1H), 7.91 (ddd, J=8.0, 2.1, 1.7 Hz, 1H), 7.38 (ddd, J=8.0, 5.0, 0.8 Hz, 1H).

후처리

  1. additionThen the reaction mixture was poured on the top of a column of silica gel
  2. washeluted with cHex/EtOAc (2:1

출처 및 근거

ORD 기록
ord-0d34f7fa59744093863db6505d5c49f8
출처 데이터셋
uspto-grants-2011_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07973039B2

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