HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → 6-Ethylthio-3-hepten-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | 1-(Triphenylphosphoranylidene)acetone | HCID 15038 | — |
| Reactant | 3-(Ethylsulfanyl)butanal | HCID 160141 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 6-Ethylthio-3-hepten-2-one | HCID 54457611 | — |
Reaction Steps
1-Triphenylphosphoranylidene-2-propanone (12.77 g, 40.0 mmol) is added to a solution of 3-(ethylthio)butyraldehyde (5.30 g, 40.0 mmol) in dichloromethane (100 ml) and the mixture is heated under reflux for 24 hours. The reaction mixture is cooled to room temperature, and the solvent evaporated in vacuo to give a beige solid. The crude product is taken up in a 1:1 mixture of hexane:ether (the insoluble material is discarded), and then concentrated under reduced pressure to give an orange oil which is further purified by column chromatography on silica gel to give 6-(ethylthio)hept-3-en-2-one as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08084649B2 |
| Source dataset | uspto-grants-2011_12 |
| ORD ID | ord-3c0061b074da4c3bb8dba46c2fd833e8 |
| Source note | uspto-grants-2011_12 |