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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 854292Generated: October 30, 2026

Ethyl 4-iodobenzoate → Ethyl 4-cyclopropylbenzoate

https://huagongshe.com/reaction/854292

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 4-iodobenzoateHCID 142891—
Reactantindium(III)chlorideHCID 159675—
ReactantHCID 178418630HCID 178418630—
CatalystHCID 178418476HCID 178418476—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 4-cyclopropylbenzoateHCID 23577288—

Reaction Conditions

Temperature-70 °C

Reaction Steps

Indium trichloride (2.2 g, 10 mmol) and THF (50 mL) were combined under nitrogen and cooled to −70° C. Cyclopropylmagnesium bromide solution (33 mL, 30 mmol, 0.92M) was added dropwise while maintaining the reaction temperature ≦−60° C. After the addition was complete the reaction was stirred 0.5 h with cooling then 0.5 h with the cooling bath removed. The resulting solution was added via cannula to a refluxing solution of ethyl-4-iodobenzoate (5.5 g, 20 mmol), trans-dichlorobis(triphenylphosphine)palladium(II) (421 mg, 0.60 mmol) and THF (100 mL) under nitrogen. After 24 h, the contents of the reaction flask were cooled and the solvent was removed in vactio. Water (100 mL) and 5% KHSO4 were added and the mixture was extracted with CH2Cl2 (3×100 mL). The combined organic extracts were washed with brine, dried with Na2SO4 and filtered. The filtrate was removed in vacuo and the remaining residue was purified by flash column chromatography (hexane:EtOAc 95:5) to give the 4-cyclopropyl-benzoic acid ethyl ester as an orange oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07259157B2
Source datasetuspto-grants-2007_08
ORD IDord-e4974b044fd14df0b8ee40973ca991f3
Source noteuspto-grants-2007_08