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 | Triphenylphosphine | HCID 11776 | — |
| Product | Amyl Acetate | HCID 12348 | 12.8% |
Reaction Steps
The procedures of Example 11 were followed, except that ketene was introduced at the rate of 32.0 ml/min (1.43 mmole/min) and that triphenylphosphine (0.066 g, 0.25 mmole) was dissolved in the further added n-amyl nitrite (50 ml). The reaction proceeded smoothly for three hours, during which no deactivation of the catalyst was observed. The reaction product was analyzed by gas chromatography, revealing that n-di-amyl malonate (165.6 mmoles, 64.5%) and n-amyl acetate (32.9 mmoles, 12.8%) were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04539423 |
| Source dataset | uspto-grants-1985_09 |
| ORD ID | ord-671fec72dd4e4503ac4eb288834dc9c9 |
| Source note | uspto-grants-1985_09 |