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diethyl (4-ethylcyclohexanon-3-yl)malonate

Base Information Edit
  • Chemical Name:diethyl (4-ethylcyclohexanon-3-yl)malonate
  • CAS No.:274931-17-8
  • Molecular Formula:C15H24O5
  • Molecular Weight:284.353
  • Hs Code.:
  • Mol file:274931-17-8.mol
diethyl (4-ethylcyclohexanon-3-yl)malonate

Synonyms:diethyl (4-ethylcyclohexanon-3-yl)malonate

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Chemical Property of diethyl (4-ethylcyclohexanon-3-yl)malonate Edit
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Technology Process of diethyl (4-ethylcyclohexanon-3-yl)malonate

There total 4 articles about diethyl (4-ethylcyclohexanon-3-yl)malonate 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:
diethyl malonate; With sodium ethanolate; In ethanol; at 0 ℃; for 0.25h;
4-ethyl-2-cyclohexen-1-one; In ethanol; at 20 ℃; for 16h;
DOI:10.1002/jhet.5570370103
Guidance literature:
Multi-step reaction with 4 steps
1.1: 78 percent / bromine / 20 °C
2.1: 79 percent / sodium methoxide / dimethylsulfoxide / 4 h / 80 °C
3.1: 74 percent / 5 percent H2SO4 / dioxane / 0.5 h / 20 °C
4.1: sodium ethylate / ethanol / 0.25 h / 0 °C
4.2: 95 percent / ethanol / 16 h / 20 °C
With sulfuric acid; bromine; sodium methylate; sodium ethanolate; In 1,4-dioxane; ethanol; dimethyl sulfoxide; 1.1: Cycloaddition / 2.1: Dehydrobromination / 3.1: Hydrolysis / 4.1: Metallation / 4.2: Addition;
DOI:10.1002/jhet.5570370103
Guidance literature:
Multi-step reaction with 2 steps
1.1: 74 percent / 5 percent H2SO4 / dioxane / 0.5 h / 20 °C
2.1: sodium ethylate / ethanol / 0.25 h / 0 °C
2.2: 95 percent / ethanol / 16 h / 20 °C
With sulfuric acid; sodium ethanolate; In 1,4-dioxane; ethanol; 1.1: Hydrolysis / 2.1: Metallation / 2.2: Addition;
DOI:10.1002/jhet.5570370103
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