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(R)-2-butyl-2-methylcyclohexanone

Base Information
  • Chemical Name:(R)-2-butyl-2-methylcyclohexanone
  • CAS No.:83606-10-4
  • Molecular Formula:C11H20O
  • Molecular Weight:168.279
  • Hs Code.:
(R)-2-butyl-2-methylcyclohexanone

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Chemical Property of (R)-2-butyl-2-methylcyclohexanone
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Technology Process of (R)-2-butyl-2-methylcyclohexanone

There total 8 articles about (R)-2-butyl-2-methylcyclohexanone which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With sodium hydroxide; In methanol; at 60 ℃; for 4h; Yield given. Yields of byproduct given. Title compound not separated from byproducts;
DOI:10.1021/jo00058a046
Guidance literature:
With sodium hydroxide; In methanol; at 60 ℃; for 4h; Yield given. Yields of byproduct given. Title compound not separated from byproducts;
DOI:10.1021/jo00058a046
Guidance literature:
Multi-step reaction with 7 steps
2: 95 percent / 2) 40percent potassium hydroxide / 1) a) petroleum/ether, 20 deg C, 15 min, b) 4 h, 2) a) 4 h, b) methanol/water, 16 h
3: bromine / CCl4 / 0 °C
4: 84 percent / potassium t-butoxide / 2-methyl-propan-2-ol / 10 h / 10 °C
5: 67 percent / sodamide / 1) petroleum ether, 2) without solvent, 130 deg C
6: 94 percent / 1) oxalyl chloride, dimethyl sulphoxide, 2) triethylamine / CH2Cl2 / 1) -67 deg C, 20 min, 2) warming to room temperature
7: H2 / 5percent palladium charcoal / ethanol / 0.17 h
With potassium hydroxide; oxalyl dichloride; potassium tert-butylate; hydrogen; bromine; sodium amide; dimethyl sulfoxide; triethylamine; palladium on activated charcoal; In tetrachloromethane; ethanol; dichloromethane; tert-butyl alcohol;
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