HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 2,3-Dihydro-2-(methylthio)-1H-inden-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Methanethiol | HCID 878 | — |
| Reactant | 2-Bromo-1-indanone | HCID 137203 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2,3-Dihydro-2-(methylthio)-1H-inden-1-one | HCID 12067526 | 38% |
Reaction Steps
After 10 g of 2-bromo-1-indanone was dissolved into 50 ml of ethanol, 25 ml of a 15% aqueous solution of a sodium salt of methylmercaptan was added dropwise thereto. After stirring for 3 hours at room temperature, the reaction mixture was poured into 300 ml of cold water. After 200 ml of ether was added thereto for extracting an organic phase, the ether layer was sequentially washed with an aqueous sodium chloride solution and water. After the ether layer was dried with magnesium sulfate, the ether was evaporated under vacuum. The residue was isolated and purified through a silica gel column (elute: hexane/ethyl acetate=7/1) to provide 3.2 g of 2-(methylthio)-1-indanone (yield: 38%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06528232B1 |
| Source dataset | uspto-grants-2003_03 |
| ORD ID | ord-b878b5739a1e4e8fa4df84e34c6711a4 |
| Source note | uspto-grants-2003_03 |