HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 854292Generated: October 30, 2026
Ethyl 4-iodobenzoate → Ethyl 4-cyclopropylbenzoate
https://huagongshe.com/reaction/854292
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl 4-iodobenzoate | HCID 142891 | — |
| Reactant | indium(III)chloride | HCID 159675 | — |
| Reactant | HCID 178418630 | HCID 178418630 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 4-cyclopropylbenzoate | HCID 23577288 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07259157B2 |
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| Source dataset | uspto-grants-2007_08 |
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| ORD ID | ord-e4974b044fd14df0b8ee40973ca991f3 |
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| Source note | uspto-grants-2007_08 |
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