HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 2,5-nonanedione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Methyl vinyl ketone | HCID 6570 | — |
| Reactant | Pentanal | HCID 8063 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Product | 2,5-nonanedione | HCID 11126503 | — |
Reaction Steps
Following the procedure described in Example 1, 13.5 g (0.05 mol) of Cat. 1, 43.1 g (0.5 mol) of n-valeraldehyde, 35.1 g (0.5 mol) of methyl vinyl ketone, 500 ml of ethanol and 20.2 g (0.2 mol) of triethylamine are heated for 12 hours under nitrogen at the reflux temperature. For working up, the solvent is distilled, the cooled residue is taken up in chloroform, the chloroform phase is washed with dilute sulphuric acid and subsequently with water, the chloroform is removed and the liquid residue is distilled in a waterpump vacuum. Nonane-2,5-dione is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04035395 |
| Source dataset | uspto-grants-1977_07 |
| ORD ID | ord-03063fefccd84353b39346574fd8c449 |
| Source note | uspto-grants-1977_07 |