HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Butanol → 1,1-Dibutoxybutane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Butanol | HCID 263 | — |
| Reactant | Decanoic Acid | HCID 2969 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 1-Butoxybut-2-ene | HCID 543904 | — |
| Product | 1,1-Dibutoxybutane | HCID 22210 | — |
| Product | HCID 347145 | HCID 347145 | — |
Reaction Steps
A glass autoclave was filled with 0.022 g of the catalyst HRuCl(CO)(PPh3)3, 0.031 g of triphenylphosphine, 0.005 g of decanoic acid, 3.18 g (24.8 mmol) of 1-butoxybut-2-ene and 1.83 g (24.8 mmol) of n-butanol. After a reaction time of 16 hours at 160° C. under autogenous pressure, the reaction mixture was analyzed by means of calibrated gas chromatography. At a conversion rate of 85%, 1,1-dibutoxybutane was formed with a selectivity of 85.1% and 1-butoxybut-1-ene with a selectivity of 10.1%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06166265 |
| Source dataset | uspto-grants-2000_12 |
| ORD ID | ord-d47679b0eea44776980cf333040af8f9 |
| Source note | uspto-grants-2000_12 |