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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDiiodomethaneHCID 6346—
ReactantMethyl 2-acetyl-3-phenylbut-3-enoateHCID 86659738—
ReactantHCID 178418750HCID 178418750—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
ProductMethyl 3-oxo-2(1-phenylcyclopropyl)butanoateHCID 8665973926%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08541455B2
Source datasetuspto-grants-2013_09
ORD IDord-7d08a98027d6459dbd05d8c9c0b06277
Source noteuspto-grants-2013_09