HuagongsheHuagongshe Chemistry Print Report · For research reference only
Heptane → Amyl Acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Heptane | HCID 8900 | — |
| Reactant | Pentyl nitrite | HCID 10026 | — |
| Reactant | Ketene | HCID 10038 | — |
| Reactant | HCID 178418416 | HCID 178418416 | — |
| Catalyst | Tetrabutylammonium Chloride | HCID 70681 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | Amyl Acetate | HCID 12348 | 18.8% |
Reaction Steps
To the same reaction vessel as in Example 9 were charged bistriphenylphosphinedibromopalladium (0.198 g, 0.25 mmole), stannous chloride (0.095 g, 0.5 mmole), tetra-n-butylammonium chloride (0.139 g, 0.5 mmole) and n-amyl nitrite (70 ml, 474.4 mmoles), together with n-heptane (150 ml) and N-methylpyrrolidone (50 ml). Then, ketene, carbon monooxide and nitrogen were introduced to the mixture at the rate of 10.1 ml/min (0.45 mmole/min), 300 ml/min and 100 ml/min, respectively, and the reaction was effected at 90° C. for 5 hours. The reaction product was analyzed by gas chromatography, revealing that di-n-amyl malonate (82.3 mmoles, 60.7%) and n-amyl acetate (25.5 mmoles, 18.8%) were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04539423 |
| Source dataset | uspto-grants-1985_09 |
| ORD ID | ord-a7cd6bdb11dd4f14b1023ffe81e65b73 |
| Source note | uspto-grants-1985_09 |