HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methane → HCID 13595902, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methane | HCID 297 | — |
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Quinone | HCID 4650 | — |
| Reactant | 1,5-Hexadiene | HCID 11598 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 13595902 | HCID 13595902 | — |
Reaction Steps
Acetoxylation of l'hexa-1,5-diene ##STR3## A 500 ml three-neck flask is charged with 15 g of hexa-1,5-diene (0.18 moles), 150 g of acetic acid, 0.77 g of benzoquinone (7 mmoles), 1 g of charcoal and 80 mg of palladium acetate (0.35 mmoles). The temperature is taken to 50°, then 7 g (0.14 moles) of 70% by weight hydrogen peroxide are introduced in 8 h, and the reaction is allowed to proceed for a further 2 h while maintaining the temperature at 50°. The acetic acid is then distilled (35°, 20×102Pa). The residue is distilled under vacuum to provide 1-acetoxy-3-methylene-cyclopentane in 65% molar yield. 1-acetoxy-3-methylene-cyclopentane
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05554786 |
| Source dataset | uspto-grants-1996_09 |
| ORD ID | ord-56a76983bb564c8da0a9820665779f30 |
| Source note | uspto-grants-1996_09 |