HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → HCID 66777786, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 66777714 | HCID 66777714 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66777786 | HCID 66777786 | 96% |
Reaction Steps
To a solution of [5-(benzyloxy)-3-methyl-1-benzofuran-2-yl](cyclohexyl)methanol (25.17 g) synthesized above in tetrahydrofuran (250 mL) was added thionyl chloride (9.44 mL) at room temperature. The reaction mixture was stirred at room temperature for 1 hr. To the reaction mixture was added aqueous sodium hydrogen carbonate solution cooled to 0° C., and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. After filtration, the filtrate was concentrated to give the title compound (25.39 g, 96%) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08436043B2 |
| Source dataset | uspto-grants-2013_05 |
| ORD ID | ord-008add1b90d3456392ee9f934058c0af |
| Source note | uspto-grants-2013_05 |