Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Peracetic Acid | HCID 6585 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Magnesium sulfate trihydrate | HCID 22242376 | — |
| Reactant | HCID 54166181 | HCID 54166181 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 57141646 | HCID 57141646 | 100% |
Reaction Steps
A mixture of 32.0 g of 1-[2,6,6-trimethyl-3-(trimethylsiloxy)-1,3-cyclohexadien-1-yl]-3-methoxy-3-methyl-1,4-pentadiene, 10.0 g of sodium hydrogen carbonate, 10.0 g of magnesium sulphate trihydrate and 500 ml of diethyl ether was stirred well at 2°-5° C., then treated dropwise with 26.45 g of 40% peracetic acid and left to warm to room temperature. The mixture was subsequently cooled to 0° C., treated dropwise with 90 ml of a mixture of methanol and 1N hydrochloric acid (vol. 1:1) and extracted with diethyl ether. The organic phase was washed twice with cold semi-concentrated sodium pyrosulphite solution, once with ice-water, twice with ice-water to which had been added a small amount of saturated sodium hydrogen carbonate solution and a further twice with ice-water. After drying over sodium sulphate and concentration under a water-jet vacuum at 35° C., there were obtained 26.4 g of crude 1-(4-hydroxy-3-oxo-2,6,6-trimethyl-1-cyclohexen-1-yl)- 3-methoxy-3-methyl-1,4-pentadiene (purity 91.5%) which still contained 7.07% of 1-(3-oxo-2,6,6-trimethyl-1-cyclohexen-1-yl)-3-methoxy-3-methyl-1,4-pentadiene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04585885 |
|---|
| Source dataset | uspto-grants-1986_04 |
|---|
| ORD ID | ord-72d7419752c441ca917f05aca4dabec1 |
|---|
| Source note | uspto-grants-1986_04 |
|---|