Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfur Dioxide | HCID 1119 | — |
| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Reactant | 5-Bromo-2,2-difluoro-1,3-benzodioxole | HCID 2736271 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 313681-67-3 | HCID 22500053 | 62.4% |
Reaction Steps
A solution of 2.37 g (10 mmol) 5-bromo-2,2-difluoro-1,3-benzodioxole in 25 ml anhydrous ether, cooled to −30° C., and 4 ml (10 mmol) n butyllithium (2.5 M in hexanes) was added at −30° C., over 10 minutes. The mixture was stirred at −30° C. for 1 hour, then sulfur dioxide gas was passed through the mixture at −20° C. for 5 minutes. The mixture then was allowed to warm up to −20° C., and the precipitate was filtered and washed with 20 ml hexane. The solid was suspended in 20 ml hexanes, 1.35 g (10 mmol) sulfuryl chloride was added, the mixture was stirred at 20° C. for 48 hours. The mixture then was filtered and the filtrate was concentrated under reduced pressure to obtain 1.6 g (62%) title compound. The product was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08455497B2 |
|---|
| Source dataset | uspto-grants-2013_06 |
|---|
| ORD ID | ord-6c24e0456c3341d4be020bf9fa2d33f4 |
|---|
| Source note | uspto-grants-2013_06 |
|---|