HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Tolyl methyl sulfone → 2-Bromo-4-(methanesulfonyl)-1-methylbenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Tolyl methyl sulfone | HCID 18521 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-Bromo-4-(methanesulfonyl)-1-methylbenzene | HCID 53216987 | 75.1% |
Reaction Steps
To a suspension of iron powder (0.0669 g, 1.20 mmol) in bromine (2.05 mL, 39.9 mmol) at 0° C. was added methyl p-tolyl sulfone (0.340 g, 2.00 mmol). The reaction was warmed up to RT and stirred for 2 h. The mixture was poured into an ice-cold 1 M solution of sodium thiosulfate and ethyl acetate. The layers were separated and the aqueous layer was extracted with ethyl acetate (3×). The combined organic layers were dried over anhydrous sodium sulfate, filtered and concentrated to give 545 mg of crude material. The crude material was purified by column chromatography (3/1 Hex/ethyl acetate to 1/1 ethyl acetate/hexanes) to give 374 mg of 2-bromo-1-methyl-4-(methylsulfonyl)benzene as a white solid. ES+=251.0 (M+H)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07759337B2 |
| Source dataset | uspto-grants-2010_07 |
| ORD ID | ord-ccfecc2491fa430cb8ec2a37f7d28238 |
| Source note | uspto-grants-2010_07 |