Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pentyl nitrite | HCID 10026 | — |
| Reactant | Ketene | HCID 10038 | — |
| Reactant | HCID 178418416 | HCID 178418416 | — |
| Catalyst | Tetrabutylammonium Chloride | HCID 70681 | — |
| Solvent | Chlorobenzene | HCID 7964 | — |
| Product | Amyl Acetate | HCID 12348 | — |
Reaction Steps
To the same reaction vessel as in Example 9 were charged bistriphenylphosphinedibromopalladium (0.396 g, 0.5 mmole), stannous chloride (0.190 g, 1 mmole), tetra-n-butylammonium chloride (0.278 g, 1 mmole) and n-amyl nitrite (25 ml, 171.0 mmole), together with monochlorobenzene (200 ml). Then, ketene, carbon monooxide and nitrogen were introduced to the mixture at the rate of 26.4 ml/min (1.18 mmole/min), 300 ml/min and 100 ml/min, respectively, and the reaction was performed at 90° C. for 3 hours. During the reaction, a further n-amyl nitrite (50 ml, 342.0 mmoles) was added dropwise to the reaction mixture over 2.5 hours. The reaction mixture was analyzed by gas chromatography, revealing that di-n-amyl malonate (125.6 mmoles, 59.1%) and n-amyl acetate (24.7 mmoles) were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04539423 |
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| Source dataset | uspto-grants-1985_09 |
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| ORD ID | ord-f06e48e88fd64a64b4bdbff37e4c7eb4 |
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| Source note | uspto-grants-1985_09 |
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