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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1670669Generated: October 30, 2026

Iodine → Ethyl 4-(4-iodophenyl)bicyclo[2.2.2]octane-1-carboxylate

https://huagongshe.com/reaction/1670669

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantSodium ThiosulfateHCID 24477—
ReactantBis(trifluoroacetoxy)iodobenzeneHCID 102317—
ReactantEthyl 4-phenylbicyclo[2.2.2]octane-1-carboxylateHCID 21627803—
SolventChloroformHCID 6212—
ProductEthyl 4-(4-iodophenyl)bicyclo[2.2.2]octane-1-carboxylateHCID 5799199887%

Reaction Steps

[Bis(trifluoroacetoxy)iodo]benzene (3.78 g, 8.78 mmol) and iodine (1.061 g, 4.18 mmol) were added to a stirred solution of ethyl 4-phenylbicyclo[2.2.2]octane-1-carboxylate (prepared according to the procedure described in WO 2007/071966) (2.16 g, 8.36 mmol, CAS 10207-26-8) in CHCl3 (50 mL). The resulting solution was stirred at ambient temperature for 90 minutes. The reaction mixture was poured into sodium thiosulfate (100 mL), extracted with DCM (2×100 mL), the organic layer was washed with aqueous sodium thiosulfate (2×80 mL), separated, dried over MgSO4, filtered and evaporated to afford a yellow oil which solidified on standing. The crude product was purified by flash silica chromatography, elution gradient 0 to 20% EtOAc in isohexane. Pure fractions were evaporated to dryness to afford the title compound (2.78 g, 87%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07994179B2
Source datasetuspto-grants-2011_08
ORD IDord-3288bfae3f49455fb376c96898be6d83
Source noteuspto-grants-2011_08