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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1719401Generated: November 1, 2026

Pentyl nitrite → Amyl Acetate

https://huagongshe.com/reaction/1719401

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPentyl nitriteHCID 10026—
ReactantKeteneHCID 10038—
ReactantHCID 178418416HCID 178418416—
CatalystTetrabutylammonium ChlorideHCID 70681—
SolventChlorobenzeneHCID 7964—
ProductAmyl AcetateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04539423
Source datasetuspto-grants-1985_09
ORD IDord-f06e48e88fd64a64b4bdbff37e4c7eb4
Source noteuspto-grants-1985_09