HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Potassium Hydroxide → alpha-Cyclohexylthiomethyl-beta-(p-methoxyphenyl)-gamma-butyrolactone
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Potassium Hydroxide | HCID 14797 | — |
| Edukt | Cyclohexanethiol | HCID 15290 | — |
| Edukt | alpha-Methanesulfonyloxymethyl-beta-(p-methoxyphenyl)-gamma-butyrolactone | HCID 20234197 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Produkt | alpha-Cyclohexylthiomethyl-beta-(p-methoxyphenyl)-gamma-butyrolactone | HCID 13518978 | 22% |
Reaktionsschritte
To a solution of 480 mg of potassium hydroxide in 40 ml of ethanol were added 2.0 g of α-methanesulfonyloxymethyl-β-(p-methoxyphenyl)-γ-butyrolactone and 1.6 ml of cyclohexylmercaptan and the resulting mixture was kept at room temperature for 4 hours. After completion of the reaction, the reaction mixture was diluted with 200 ml of ethyl ether, washed with water and saturated saline, dried over magnesium sulfate and the solvent was distilled off. The crude product thus obtained was purified by a silica gel column chromatography to give 600 mg (yield 22%) of the title compound.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04613613 |
| Quelldatensatz | uspto-grants-1986_09 |
| ORD ID | ord-ba41b964acd849fab487151f8f23f48f |
| Quellennotiz | uspto-grants-1986_09 |