HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Mercaptoethanol → HCID 15238320, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Mercaptoethanol | HCID 1567 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | 3,4-dihydro-2H-pyran | HCID 8080 | — |
| Reactant | Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1) | HCID 466102 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 15238320 | HCID 15238320 | — |
Reaction Steps
A mixed solution of 2-mercaptoethanol (25.0 g) and pyridinium p-toluenesulfonate (8.04 g) in dichloromethane (400 ml) was cooled with ice and 3,4-dihydro-2H-pyran (70 g) was gradually added. The mixture was stirred at room temperature for 3 hours. Then, 3,4-dihydro-2H-pyran (10.8 g) was further added and the mixture was stirred for an additional 3 hours. To this reaction mixture was added ether (1 l) and the organic layer was washed with aqueous sodium chloride solution and dried over anhydrous sodium sulfate and the solvent was distilled off under reduced pressure. The procedure gave 78.8 g of tetrahydropyran-2-yl 2-[(tetrahydropyran-2-yl)thio]ethyl ether as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05393751 |
| Source dataset | uspto-grants-1995_02 |
| ORD ID | ord-16bb0ae62e334fe9bc7f984dc7a43251 |
| Source note | uspto-grants-1995_02 |