HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → ethyl 2-(1-methyl-2-oxocyclopentyl)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | 2-Methylcyclopentanone | HCID 14265 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | ethyl 2-(1-methyl-2-oxocyclopentyl)acetate | HCID 12292030 | — |
Reaction Steps
A solution of sodium tert.-amylate in toluene (70 ml, 0.1 mole) is added dropwise with stirring under an atmosphere of nitrogen to a solution of 2-methylcyclopentanone (9.8 g, 0.1 mole) and ethyl bromoacetate (16.7 g, 0.1 mole) in dry benzene (100 ml). The reaction is exothermic, a precipitate is formed, and the mixture turns yellow-orange. Stirring is continued for 3 hrs. at room temperature, the solution is washed with 1% HCl, cold water, and brine, dried over anhydrous magnesium sulfate and the solvent evaporated to yield 1-methyl-2-oxocyclopentane acetic acid ethyl ester as a pale yellow oil which is used without further purification in the subsequent step and which is identical with the same compound described in Example 5.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04057559 |
| Source dataset | uspto-grants-1977_11 |
| ORD ID | ord-7a342331d404476e8fb65aada73f77cf |
| Source note | uspto-grants-1977_11 |