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23994-65-2

5-(2-Thienyl)-1,3-cyclohexanedione synthesis

3synthesis methods
-

Yield:23994-65-2 69%

Reaction Conditions:

Stage #1: 2-thenylideneacetone;diethyl malonatewith sodium in methanol at 80; for 4 h;
Stage #2: with sodium hydroxide in methanol;water at 80; for 0.666667 h;
Stage #3: with hydrogenchloride in methanol;water;Reflux;

Steps:

I

[0069] Sodium metal (1 eq., 970 mg) was dissolved in dry MeOH (20 ml). After 0.5 hours, diethylmalonate (1 eq., 6.2 ml) was added dropwise to maintain temperature between 15-20 °C; (8) is then added at 60 °C. The reaction mixture was refluxed (80 °C) for 4 hours and made alkaline with aqueous NaOH (13 ml of 17.6 grams NaOH in 70 ml H20). The alkaline solution was heated at 80 °C for 40 minutes, and then cone. HC1 (13 ml) was added under reflux. On cooling, a yellow solid (9) was obtained (5.3 grams, 69%> yield).

References:

WO2011/62964,2011,A1 Location in patent:Page/Page column 19

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