Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | Ethyl 4-oxoheptanoate | HCID 12271529 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | 2-Ethylcyclopentane-1,3-dione | HCID 69978 | 46% |
Reaction Steps
A 1 l. three-necked flask, equipped with a dropping funnel, mechanical stirrer and a distillation head with thermometer and Liebig condenser was charged with 515 ml of xylene (b.p. 138°-140°), stirred and heated to boiling. 65.9 g of a 24% (wt/wt) sodium methoxide solution (prepared as in Example 1) in methyl alcohol (15.8 g = 0.293 moles) was added over 10 min., distilling off continuously the methyl alcohol. 300 ml of additional xylene were added and distillation was continued until the vapor temperature reached 135°. After the addition of 6.6 ml of dimethylsulfoxide, a solution of 40 g (0.232 moles) of 4-oxoheptanoic acid ethyl ester in 80 ml of xylene was added over 25 min. to the vigorously stirred sodium methoxide suspension while keeping the vapor temperature at ca. 135°C by continuous distillation of xylene. The orange-colored mixture was stirred and heated for an additional 5 min. and then allowed to cool to room temperature. Water was added, the mixture was acidified and the product filtered, washed, dried and recrystallized from water to afford 13.45 g (46%) of 2-ethyl-cyclopentan-1,3-dione, m.p. (uncorr.): 171°-172°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03931322 |
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| Source dataset | uspto-grants-1976_01 |
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| ORD ID | ord-00e9a7a80a3849f585a644732f770b14 |
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| Source note | uspto-grants-1976_01 |
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