HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → 1-Bromo-4-(methylsulphinyl)benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 4-Bromothioanisole | HCID 66037 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-Bromo-4-(methylsulphinyl)benzene | HCID 3013958 | — |
Reaction Steps
4.06 g (20 mmol) of 4-bromothioanisole and 75 ml of dichloromethane were introduced into a round-bottomed flask and 6.3 g (20 mmol) of meta-chloroperbenzoic acid were added. Stirring was carried out at room temperature for four hours and the reaction mixture was poured into water. The organic phase was separated by settling, dried over magnesium sulfate and evaporated. The residue obtained was purified by chromatography on a silica column eluted with a mixture of dichloromethane and heptane (70/30). After evaporating the solvents, 1.22 g (28%) of the expected sulfoxide, with a melting point of 80°-81° C., was recovered.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05716624 |
| Source dataset | uspto-grants-1998_02 |
| ORD ID | ord-6fba4f6b6efb461e92bb0e1d5cb1e036 |
| Source note | uspto-grants-1998_02 |