HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 45230Generated: October 29, 2026
Water → Methyl 3-oxo-2(1-phenylcyclopropyl)butanoate
https://huagongshe.com/reaction/45230
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Diiodomethane | HCID 6346 | — |
| Reactant | Methyl 2-acetyl-3-phenylbut-3-enoate | HCID 86659738 | — |
| Reactant | HCID 178418750 | HCID 178418750 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 3-oxo-2(1-phenylcyclopropyl)butanoate | HCID 86659739 | 26% |
Reaction Steps
To a solution of 1 g (4.6 mmol) of methyl 2-acetyl-3-phenylbut-3-enoate in 16 mL of DCM are successively added dropwise 20.8 mL (22.9 mmol) of a 1.1M solution of diethylzinc in toluene and 3.7 mL (45.8 mmol) of diiodomethane. The reaction medium is refluxed for 18 hours. After cooling to room temperature, the reaction mixture is treated with 100 mL of water and then extracted with DCM (3×100 mL). The organic phases are combined, washed successively with water (4×100 mL) and brine (100 mL), 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 95/5 cyclohexane/EtOAc mixture. 280 mg of methyl 3-oxo-2(1-phenylcyclopropyl)butanoate are obtained in the form of a yellow 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-7d08a98027d6459dbd05d8c9c0b06277 |
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| Source note | uspto-grants-2013_09 |
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