HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 45218Generated: October 29, 2026
Acetone → Methyl 2-acetyl-3-methylbut-2-enoate
https://huagongshe.com/reaction/45218
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Methyl acetoacetate | HCID 7757 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 2-acetyl-3-methylbut-2-enoate | HCID 12576903 | — |
Reaction Steps
To a mixture of 9.54 g (70 mmol) of anhydrous ZnCl2, 53.9 mL (500 mmol) of methyl acetoacetate and 55 mL (750 mmol) of acetone are added 64 mL of acetic anhydride. The reaction medium is then heated for 3 days at 50° C., and then diluted with 1 L of DCM and washed with water (3×100 mL). The organic phase is dried over Na2SO4, filtered and then concentrated under reduced pressure. The residue obtained is purified by chromatography on a column of silica gel, eluting with a cyclohexane/EtOAc gradient of 0 to 10% EtOAc. After concentrating under reduced pressure, 51.5 g of methyl 2-acetyl-3-methylbut-2-enoate are obtained in the form of a colourless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08541455B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-021e21ec760642d9bbc63f16bf9d6188 |
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| Source note | uspto-grants-2013_09 |
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