HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodine → 1-Benzenesulfonyl-2-(4-bromo-phenyl)-aziridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 4-Bromostyrene | HCID 16263 | — |
| Reactant | Chloramine B | HCID 4347343 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1-Benzenesulfonyl-2-(4-bromo-phenyl)-aziridine | HCID 46845669 | 48.7% |
Reaction Steps
To a stirred suspension of chloramine B (CAS [127-52-6], 1.35 g) in acetonitrile (18 mL) under argon was added iodine (0.16 g). 4-Bromostyrene (2.41 g) was added and the mixture was stirred for 19 h at room temperature. Dichloromethane (240 mL) and water (120 mL) were added and the mixture was extracted with dichloromethane. The org. phase was washed with water and brine, dried over MgSO4 and K2CO3 and filtered. The filtrate was concentrated and the product was purified using column chromatography (SiO2, cyclohexane/ethyl acetate 95:5=>ethyl acetate) to give 1-benzenesulfonyl-2-(4-bromo-phenyl)-aziridine (1.04 g) as a colorless oil. MS: 340.0 ([M+H]+)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08063088B2 |
| Source dataset | uspto-grants-2011_11 |
| ORD ID | ord-544429e502314da8a3d57eaade455ae0 |
| Source note | uspto-grants-2011_11 |