HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,4-Dioxane → HCID 21841477, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | Boronic Acid | HCID 61668 | — |
| Reactant | Potassium Bromide | HCID 253877 | — |
| Reactant | HCID 21841495 | HCID 21841495 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Product | HCID 21841477 | HCID 21841477 | — |
Reaction Steps
A mixture of 3 g of the product of Stage A, 1.66 g of boronic acid (Preparation 5), 3.5 g of monohydrated potassium phosphate, 1.32 g of potassium bromide and 300 mg of Pd(PPh3)4 (palladium tetrakis) in 50 ml of dioxane was refluxed for 12 hours. After pouring the reaction medium into a water-ice mixture, and carrying out extraction with ethyl acetate, the organic phase was dried, filtered and evaporated under reduced pressure. The crude product was purified by chromatography, eluting with a cyclohexane/ethyl acetate mixture (85/15) to obtain 1.95 g of the expected product with a Rf=0.05 (cyclohexane/ethyl acetate 85/15).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05827887 |
| Source dataset | uspto-grants-1998_10 |
| ORD ID | ord-dfd394d5458c48b9b266d113607b4bf0 |
| Source note | uspto-grants-1998_10 |