HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thiophenol → 4-phenylsulfanyl-[1,3]dioxolan-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thiophenol | HCID 7969 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Vinylene carbonate | HCID 13385 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-phenylsulfanyl-[1,3]dioxolan-2-one | HCID 11287057 | — |
Reaction Steps
In 70 mL of tetrahydrofuran (THF), 3 g of vinylene carbonate and 5.1 g of benzenethiol were dissolved, and then 4.7 g of triethylamine was added. The mixture was refluxed under an argon atmosphere for 4 hours. When the reaction was finished, the solvent was removed through distillation under reduced pressure, and the resulting material was subjected to the column chromatography on silica gel (eluted with 20% hexane/ethylacetate) and purified to obtain a target product, 4-phenylsulfanyl-[1,3]dioxolan-2-one.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07037624B2 |
| Source dataset | uspto-grants-2006_05 |
| ORD ID | ord-0756cdc0e6a8450e9993aa36a63b75ac |
| Source note | uspto-grants-2006_05 |