HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → HCID 68514363, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 68511594 | HCID 68511594 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 68514363 | HCID 68514363 | 92% |
Reaction Steps
To a solution of 4-{4-[cyclohexyl(hydroxy)methyl]-5-ethylthiophen-2-yl}tetrahydro-2H-thiopyran-4-ol (532 mg) synthesized in Example 85 (3) in toluene (10 mL) was added thionyl chloride (137 μL), and the mixture was stirred at room temperature for 1 hr. The reaction mixture was poured into ice-cooled saturated aqueous sodium hydrogen carbonate solution, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over magnesium sulfate and concentrated under reduced pressure to give the title compound (491 mg, 92%) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08309580B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-9c1f1b6639c44b2d81828ec32c224ce2 |
| Source note | uspto-grants-2012_11 |