HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Chloride → Methyl 3-oxo-7,11-dimethyl-dodeca-6,10-dienoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Dimethyl Carbonate | HCID 12021 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Geranylacetone | HCID 1549778 | — |
| Solvent | toluene N-methylpyrrolidone | HCID 21877177 | — |
| Product | Methyl 3-oxo-7,11-dimethyl-dodeca-6,10-dienoate | HCID 53708905 | — |
Reaction Steps
24 g (0.55M) of sodium hydride (55% dispersion in mineral oil) were added at 20° under nitrogen to a solution of 135 g (1.5M) of dimethylcarbonate in 500 ml of a mixture of toluene/N-methylpyrrolidone (9:1). The obtained mixture was heated to reflux (bath temperature 100°) then, during 1 h, there was added a solution of 0.5M of geranylacetone in 135 g (1.5M) of dimethylcarbonate, where upon the resulting reaction mixture was kept refluxing during 10 min. It was finally poured into a 10% aqueous solution of NH4Cl saturated with NaCl. An ether extraction, followed by the usual work up of the combined organic extracts and fractional distillation gave methyl 3-oxo-7,11-dimethyl-dodeca-6,10-dienoate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05453525 |
| Source dataset | uspto-grants-1995_09 |
| ORD ID | ord-fe80c16b71244bbe8c598eaaf4a7b2b5 |
| Source note | uspto-grants-1995_09 |