HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Hydroxybenzenethiol → 3-[(tetrahydro-2H-pyran-4-ylmethyl)sulfanyl]phenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Hydroxybenzenethiol | HCID 2736613 | — |
| Reactant | 4-(Bromomethyl)oxane | HCID 2773286 | — |
| Reactant | Sodium methanolate methanol | HCID 23694274 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-[(tetrahydro-2H-pyran-4-ylmethyl)sulfanyl]phenol | HCID 59527237 | 59.6% |
Reaction Steps
3-Sulfanylphenol (250 mg) was dissolved in methanol (5 mL), and a 28% sodium methoxide-methanol solution (0.5 mL) was added thereto, followed by stirring at room temperature for 10 minutes. 4-(Bromomethyl)tetrahydro-2H-pyrane (410 mg) was added to the reaction mixture, followed by stirring at room temperature for 3 hours. The solvent was evaporated under reduced pressure, and then water was added to the residue, followed by extraction with ethyl acetate. The organic layer was washed with saturated brine and dried. The solvent was evaporated under reduced pressure, and the residue was washed with hexane to obtain 3-[(tetrahydro-2H-pyran-4-ylmethyl)sulfanyl]phenol (265 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08367702B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-a50ed59e16d641e1a36b653522c88244 |
| Source note | uspto-grants-2013_02 |