HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydroxide → Estrone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydroxide | HCID 961 | — |
| Reactant | Estrone | HCID 5870 | — |
| Reactant | Dimethyl Sulfate | HCID 6497 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Estrone | HCID 5870 | — |
| Product | Dimethyl Ether | HCID 8254 | — |
Reaction Steps
Into a mixture of 1 g of estrone, 0.5 ml of dimethyl sulfate and 5 ml of tetrahydrofuran, 6 ml of 10% methanolpotassium hydroxide solution was added over a period of 1 hour. The reaction temperature was maintained at 10° - 15°C. The resulting mixture was stirred for one hour to complete the etherification. Then, 15 ml of water was added to the reaction mixture, tetrahydrofuran and methanol were distilled off under atmospheric pressure. The residue was extracted with chloroform, washed with water, and dried. Evaporation of chloroform yielded 1.032 g of the 100% purity methyl ether of estrone in a 98.4% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03939186 |
| Source dataset | uspto-grants-1976_02 |
| ORD ID | ord-9a019c57b832489c8cae04cf983fe665 |
| Source note | uspto-grants-1976_02 |