HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 21485432, compound → 2-Ethylcyclopentane-1,3-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 21485432 | HCID 21485432 | — |
| Reactant | HCID 21485715 | HCID 21485715 | — |
| Solvent | Potassium Hydroxide | HCID 14797 | — |
| Product | 2-Ethylcyclopentane-1,3-dione | HCID 69978 | — |
Reaction Steps
Reflux 6-(3,5-dimethoxyphenyl)hex-1-en-3-one, containing a small amount of 6-(3,5-dimethoxyphenyl)-1-diethylaminohexan-3-one (6 g, produced by slow distillation of the latter substance) with 2-ethylcyclopentane-1,3-dione (3.5 g) in 0.12% anhydrous methanolic potassium hyroxide (10 cc) for 10 hours. Work up the reaction mixture as for the preparation of 2-(6 -m-acetoxyphenyl-3-oxohexyl)-2-methylcyclopentane-1,3-dione to obtain 2-[6-(3,5-dimethoxyphenyl)-3-oxohexyl]-2-ethylcyclopentane-1,3-dione as a viscous gum; infrared absorption peaks at 5.80, 6.25 μ (split peak).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04002746 |
| Source dataset | uspto-grants-1977_01 |
| ORD ID | ord-ae8fb202621245eea4aff0cf924584f6 |
| Source note | uspto-grants-1977_01 |