HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → (R,R)-Stilbene oxide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | trans-Stilbene | HCID 638088 | — |
| Reactant | Potassium hydroxy sulfite | HCID 23707502 | — |
| Catalyst | Tetrabutylammonium hydrogen sulfate | HCID 94433 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | EDTA disodium salt | HCID 8759 | — |
| Product | (R,R)-Stilbene oxide | HCID 185583 | 85% |
Reaction Steps
Reaction at 20° C.: trans-Stilbene (0.181 g, 1 mmol) was dissolved in acetonitrile/DMM (15 mL, ½, V/V). subsequently were added buffer (10 mL, 0.05 M solution of Na2B4O7.H2O in 4×10−4 M aqueous Na2EDTA), tetrabutylammonium hydrogen sulfate (0.015 g, 0.04 mmol), and ketone 1 (0.0774 g, 0.3 mmol). A solution of Oxone® (1.0 g, 1.6 mmol) in aqueous Na2EDTA (4×10−4 M, 6.5 mL) and a solution of K2CO3 (0.93 g, 6.74 mmol) in water (6.5 mL) were added dropwise separately over a period of 30 min (via additional funnels). The reaction was then worked up by the same procedure as Method A to afford trans-stilbene oxide (0.166 g, 85% yield, 97.9%ee).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06348608B1 |
| Source dataset | uspto-grants-2002_02 |
| ORD ID | ord-35b3001d8fd14f139dd9c222b85cf3e0 |
| Source note | uspto-grants-2002_02 |