HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → 1-(Ethylsulfinyl)-4-nitrobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Sodium Thiosulfate Pentahydrate | HCID 61475 | — |
| Reactant | Metaperiodic acid | HCID 65185 | — |
| Reactant | 1-(Ethylsulfanyl)-4-nitrobenzene | HCID 12321339 | — |
| Catalyst | Iron chloride (FeCl3) | HCID 24380 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1-(Ethylsulfinyl)-4-nitrobenzene | HCID 279146 | 68% |
Reaction Steps
428 mg (2.64 mmol) of iron(III) chloride was added to a mixture of 16.86 g (92.02 mmol) of 1-ethylsulfanyl-4-nitrobenzene in 75 ml acetonitrile and it was stirred for 10 minutes at room temperature. Then 22.44 g (98.44 mmol) of periodic acid was added in portions, so that the temperature did not exceed 30° C. The mixture was stirred for 50 minutes and was then added, with stirring, to a mixture of 170 ml DCM, 500 ml ice water and 100 g sodium thiosulfate pentahydrate. It was extracted with DCM (2×). The combined organic phases were dried (Na2SO4), filtered and concentrated by evaporation. The residue obtained was recrystallized from ethyl acetate/hexane. 12.49 g (62.69 mmol; yield: 68%) of the product was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08735412B2 |
| Source dataset | uspto-grants-2014_05 |
| ORD ID | ord-54a575e599ac45c5ae1f9cc7cb9a8cfb |
| Source note | uspto-grants-2014_05 |