HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pentyl nitrite → Amyl Acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pentyl nitrite | HCID 10026 | — |
| Reactant | Ketene | HCID 10038 | — |
| Reactant | HCID 178418416 | HCID 178418416 | — |
| Solvent | Chlorobenzene | HCID 7964 | — |
| Product | Amyl Acetate | HCID 12348 | 28.3% |
Reaction Steps
To the same reaction vessel as in Example 9 were charged bistriphenylphosphinedibromopalladium (0.791 g, 1 mmole), stannous bromide (0.558 g, 2 mmoles) and tetra-n-ethylammonium bromide (0.420 g, 2 mmoles), together with n-amyl nitrite (50 ml, 356.0 mmoles) and chlorobenzene (200 ml). Then, nitrogen gas containing 10.0 vol.% of ketene and carbon monooxide were introduced to the mixture at the rate of 116.1 ml/min and 200 ml/min, respectively, and the reaction was performed at 90° C. for 3 hours. The reaction mixture was analyzed to reveal that di-n-amyl malonate (63.0 mmoles, 49.4%) and n-amyl acetate (36.5 mmoles, 28.3%) were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04539423 |
| Source dataset | uspto-grants-1985_09 |
| ORD ID | ord-b705953890c14bcbb6e34580fdd964c9 |
| Source note | uspto-grants-1985_09 |