HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → 2-(1-Chloro-3-methylbutyl)-5-methoxy-3-methyl-1-benzofuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1-(5-Methoxy-3-methyl-1-benzofuran-2-yl)-3-methylbutan-1-ol | HCID 66777775 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-(1-Chloro-3-methylbutyl)-5-methoxy-3-methyl-1-benzofuran | HCID 66778218 | 94% |
Reaction Steps
To a solution (10 mL) of 1-(5-methoxy-3-methyl-1-benzofuran-2-yl)-3-methylbutan-1-ol (761 mg) synthesized above in toluene were added pyridine (297 μL) and thionyl chloride (268 μL), and the mixture was stirred at room temperature for 3 hr. Saturated aqueous sodium hydrogen carbonate solution was added to quench the reaction, and the reaction 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 object compound (769 mg, 94%) as a brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08436043B2 |
| Source dataset | uspto-grants-2013_05 |
| ORD ID | ord-f894c2d06abe48b0944b97c5cb90df45 |
| Source note | uspto-grants-2013_05 |