HuagongsheHuagongshe Chemistry Print Report · For research reference only
Homoallyl bromide → Bisbutenyl mercury
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Homoallyl bromide | HCID 21241 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | Bis(3-butenyl)mercury | HCID 12533408 | — |
| Reactant | HCID 178418797 | HCID 178418797 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Bisbutenyl mercury | HCID 86745677 | 60% |
Reaction Steps
Preparation of bis(3-butenyl)mercury: To a solution of 3-butenylmagnesium bromide, prepared from 25 g of 1-bromo-3-butene (187 mmole) and 5 g of magnesium (208 mmole) in 40 mL of tetrahydrofuran, was added dropwise, at 50° C. with stirring, a solution of 25.2 g of mercuric chloride (93 mmole) in tetrahydrofuran. After stirring for 2 hours at 60° C., the reaction mixture was hydrolyzed with water at 0°-5° C. Organic layer was separated from aqueous layer; the product was distilled to give bisbutenyl mercury in 60% yield. The yield of the desired product was confirmed by gas chromatography (GC) and 1H NMR.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05192616 |
| Source dataset | uspto-grants-1993_03 |
| ORD ID | ord-c734b09e9cf34009a087b33304658c33 |
| Source note | uspto-grants-1993_03 |