HuagongsheHuagongshe Chemistry Print Report · For research reference only
6-Bromo-2,2-dimethyl-2H-chromene → 2,2-Dimethyl-6-phenylsulfanyl-2H-chromene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 6-Bromo-2,2-dimethyl-2H-chromene | HCID 11770533 | — |
| Reactant | Benzene disulfide | HCID 86611018 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2,2-Dimethyl-6-phenylsulfanyl-2H-chromene | HCID 10539863 | — |
Reaction Conditions
| Temperature | -78 °C |
|---|
Reaction Steps
6-Bromo-2,2-dimethyl-2H-chromene (10 mmoL) in THF (20 mL) was treated with n-butyl lithium (15 mmoL) dropwise at −78° C. The resulting solution was stirred at −78° C. for 30 min. Benzene disulfide (10 mmoL) in THF (10 mL) was then added dropwise into the reaction over about 15 min. The reaction mixture was kept at −78° C. and slowly warmed to room temperature over 2 hrs. The solvent was removed and the residue was partitioned between diethyl ether and water. The combined organic layer was washed with brine, filtered, dried over anhydrous Na2SO4 and concentrated to yield crude material, which was purified by silica gel chromatography to yield the title compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07812183B2 |
| Source dataset | uspto-grants-2010_10 |
| ORD ID | ord-c252170d81594bea9745d65e9aabfa23 |
| Source note | uspto-grants-2010_10 |