HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 1-(Benzyloxy)-4-[(trans)-2-nitrocyclopropyl]benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | Sulfoxonium, trimethyl-, iodide (1:1) | HCID 74498 | — |
| Reactant | (E)-1-(Benzyloxy)-4-(2-nitrovinyl)benzene | HCID 5702926 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 1-(Benzyloxy)-4-[(trans)-2-nitrocyclopropyl]benzene | HCID 66629098 | 26% |
Reaction Steps
Trimethylsulfoxonium iodide (0.62 g, 2.82 mmol) was added in portions to a solution of t-BuOH (0.32 g, 2.82 mmol) in dry DMSO (5 mL). After 10 min a solution of 1-(benzyloxy)-4-[(E)-2-nitrovinyl]benzene (0.60 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 orange oil was purified by column chromatography on silica gel (5% EtOAc/hexanes) affording 0.16 g of 1-(benzyloxy)-4-[(trans)-2-nitrocyclopropyl]benzene [Rf=0.5 (20% EtOAc/hexanes), white solid, 26% yield].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08722743B2 |
| Source dataset | uspto-grants-2014_05 |
| ORD ID | ord-d52e6ec1b39e47e4951522d9d30c2273 |
| Source note | uspto-grants-2014_05 |