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2-Iso-butylcyclopentanone synthesis

7synthesis methods
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Yield:4668-65-9 65 %Chromat.

Reaction Conditions:

with hydrogen at 140; under 26252.6 Torr; for 6.66667 h;Autoclave;

Steps:

2.4. One-pot synthesis of 2-alkyl cycloketones from aldehydes andcycloketones

General procedure: Take 2BCH as example, 18 g (0.25 mol) n-butanal, 54 g (0.55 mol)cyclohexanone, and 3.7 g catalysts were added into a 250 mL autoclave.Oxygen in autoclave was displaced thrice by 0.2 MPa N2 and 0.5 MPa H2in sequence. Then, 3.5 MPa H2 was charged into the autoclave at roomtemperature. The reaction was carried out at 140 C for 400 min understirring at 400 rpm followed by cooling to room temperature naturally.The other 2-alkyl cycloketones were synthesized with the same cycloketone/aldehyde molar ratio.

References:

Xue, Weiyang;Gu, Bin;Wu, Huiling;Liu, Mengyang;He, Songbo;Li, Jingmei;Rong, Xin;Sun, Chenglin [Applied Catalysis A: General,2021,vol. 616,art. no. 118107]

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