HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → Butanal
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Vinyloxirane | HCID 13586 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | Butanal | HCID 261 | — |
| Product | 1,2-Epoxybutane | HCID 7834 | — |
Reaction Steps
In an autoclave having a capacity of 50 ml, the solution to be hydrogenated comprising 2.5 g of vinyloxirane and 22.5 g of tetrahydrofuran was admixed with 0.5 g of catalyst No. 1 without prior activation with hydrogen and hydrogenated with hydrogen at 25° C. and 40 bar for 8 hours while stirring. At a conversion of 100%, 91.7 mol% of 1,2-butylene oxide, 1.0 mol% of n-butyraldehyde and 2.6 mol% of n-butanol were obtained. Examples 3-22
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05948921 |
| Source dataset | uspto-grants-1999_09 |
| ORD ID | ord-383cfefa279543b0833fe8bbe711aea4 |
| Source note | uspto-grants-1999_09 |