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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | Bis(trifluoroacetoxy)iodobenzene | HCID 102317 | — |
| Reactant | Ethyl 4-phenylbicyclo[2.2.2]octane-1-carboxylate | HCID 21627803 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | Ethyl 4-(4-iodophenyl)bicyclo[2.2.2]octane-1-carboxylate | HCID 57991998 | 87% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07994179B2 |
|---|
| Source dataset | uspto-grants-2011_08 |
|---|
| ORD ID | ord-3288bfae3f49455fb376c96898be6d83 |
|---|
| Source note | uspto-grants-2011_08 |
|---|