HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 1-Bromo-4-[(trans)-2-nitrocyclopropyl]benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sulfoxonium, trimethyl-, iodide (1:1) | HCID 74498 | — |
| Reactant | trans-4-Bromo-beta-nitrostyrene | HCID 688204 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 1-Bromo-4-[(trans)-2-nitrocyclopropyl]benzene | HCID 67064639 | 27% |
Reaction Steps
Trimethylsulfoxonium iodide (0.62 g, 2.82 mmol) was added in portions to a solution of t-BuOK (0.32 g, 2.82 mmol) in dry DMSO (5 mL). After 10 min a solution of 1-bromo-4-[(trans)-2-nitrovinyl]benzene (0.53 g, 2.35 mmol) in DMSO (5 mL) was transferred via canula and the mixture was stirred at room temperature for 6 h. The reaction was poured over water (10 mL) and extracted with Et2O (3×10 mL); the organic layers were washed with brine (2×15 mL), dried over anhydrous Na2SO4 and filtered. After removal of the solvent, the residual oil was purified by column chromatography on silica gel (5% EtOAc/hexanes) affording 0.15 of 1-bromo-4-[(trans)-2-nitrocyclopropyl]benzene [27% yield].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08946296B2 |
| Source dataset | uspto-grants-2015_02 |
| ORD ID | ord-bf0e34c50e5441799b393716139565b7 |
| Source note | uspto-grants-2015_02 |