HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → Dimethyl (2-methoxy-phenylsulphanyl)malonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Thioguaiacol | HCID 23642 | — |
| Reactant | Dimethyl chloromalonate | HCID 120070 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Dimethyl (2-methoxy-phenylsulphanyl)malonate | HCID 22362038 | — |
Reaction Steps
1 g of KOH was added to a solution of 2.2 ml of 2-methoxythiophenol in 30 ml of ethanol. The reaction mixture was treated at room temperature with a solution of dimethyl chloromalonate in 5 ml of ethanol, stirred for 1 hour and evaporated. The residue was partitioned between ether and water. The organic phase was dried, concentrated and the residue was purified over silica gel with methylene chloride. 3.6 g of dimethyl (2-methoxy-phenylsulphanyl)malonate, MS: M=270, were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05420129 |
| Source dataset | uspto-grants-1995_05 |
| ORD ID | ord-19e57d3a32fb454487ce6ca1e155c744 |
| Source note | uspto-grants-1995_05 |