HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → 1-Methoxyoct-2-ene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 1-Methoxy-2,7-octadiene | HCID 535026 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Tris(triphenylphosphine)ruthenium(II) dichloride | HCID 84971 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-Methoxyoct-2-ene | HCID 54009999 | — |
Reaction Steps
1000 g of 1-methoxy-2,7-octadiene, 500 ml of tetrahydrofuran, 500 ml of ethanol and 2.5 g of tris(triphenylphosphine)ruthenium(II) chloride were placed in a 3 l Büchi autoclave. The temperature was set to 30° C. and the autoclave was pressurized to 30 bar by means of hydrogen. The reaction was followed via the amount of hydrogen taken up and by means of GC analyses. After 6 hours, the reaction was stopped. According to GC analysis, 98% of the 1-methoxy-2,7-octadiene had reacted to form 1-methoxy-2-octene (cis and trans) with a selectivity of 89%. The 1-methoxy-2-octene was separated from solvents and catalyst by distillation.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07030286B2 |
| Source dataset | uspto-grants-2006_04 |
| ORD ID | ord-feb857e726424950acdea963b88e41cc |
| Source note | uspto-grants-2006_04 |