HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 890696Generated: October 26, 2026
Potassium Iodide → Methyl 2-acetylhexanoate
https://huagongshe.com/reaction/890696
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Butyl bromide | HCID 8002 | — |
| Reactant | sodium (2E)-4-methoxy4-oxo-2-buten-2-olate | HCID 23681258 | — |
| Solvent | 2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl- | HCID 81646 | — |
| Product | Methyl 2-acetylhexanoate | HCID 12527573 | — |
Reaction Steps
30 g (217 mmol) of sodium (2E)-4-methoxy-4-oxo-2-buten-2-olate (Example 13A) suspended in 1,3-dimethyltetrahydro-2(1H)-pyrimidone and 1.24 g (7.5 mmol) of potassium iodide are treated dropwise with 29.8 g (217 mmol) of butyl bromide and the mixture is stirred at 80° C. for 1 h under reflux. The cooled mixture is then added to ice water and extracted with diethyl ether. The ether phase is washed with sodium thiosulphate solution, dried, concentrated and chromatographed. The eluent used is cyclohexane having an increasing ethyl acetate content.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06998402B2 |
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| Source dataset | uspto-grants-2006_02 |
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| ORD ID | ord-d000757376de4d02a6ce64ed2ce04c11 |
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| Source note | uspto-grants-2006_02 |
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