HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2390754Generated: October 30, 2026
Isopropanol → Propan-2-yl 4-methyl-3-oxopentanoate
https://huagongshe.com/reaction/2390754
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Methyl 4-methyl-3-oxopentanoate | HCID 2759969 | — |
| Product | Propan-2-yl 4-methyl-3-oxopentanoate | HCID 57643949 | 83% |
Reaction Steps
Methyl 4-methyl-3-oxo-pentanoate (304 g), isopropyl alcohol (500 ml) and p-toluenesulfonic acid (3.8 g) were stirred together and heated to reflux at 90° C. After 3 hours, 400 ml of solvent was collected by distillation at atmospheric pressure. Fresh isopropyl alcohol was added and the mixture refluxed for a further 3 hours. The cycle of distillation, addition of fresh solvent and refluxing was continued until the conversion had reached 95%, determined by a peak area ratio of product:starting material of 95:5 measured by LC. The remaining volatile solvents were removed by distillation and the resultant liquid washed with 10% sodium carbonate solution and dried over anhydrous sodium sulfate and filtered to give isopropyl 4-methyl-3-oxo-pentanoate as a clear liquid (301 g, 83%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08273878B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-a27c3ed8982247b1b4c1f5da1e9ff066 |
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| Source note | uspto-grants-2012_09 |
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