HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1166072Generated: October 29, 2026
Iodine → 1-(Benzyloxy)-2-iodo-4-(trifluoromethoxy)benzene
https://huagongshe.com/reaction/1166072
Participants
| Role | Name | HCID | Charge |
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| Reactant | Iodine | HCID 807 | — |
| Reactant | 2-Benzyloxy-5-(trifluoromethoxy)benzene | HCID 21584094 | — |
| Catalyst | Silver trifluoroacetate | HCID 76299 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(Benzyloxy)-2-iodo-4-(trifluoromethoxy)benzene | HCID 11395278 | 101.5% |
Reaction Steps
Iodine (71.96 g, 0.28 mol) in chloroform was added dropwise to a mixture of 2-benzyloxy-5-(trifluoromethoxy)benzene (Preparation 12, 73.06 g, 0.27 mol) and silver trifluoroacetate (71.57 g, 0.32 mol) in dichloromethane and the mixture was stirred at room temperature for 18 hours. The mixture was filtered through celite, washed with aqueous sodium thiosulfate (5%, 2×2 l), dried (MgSO4) and the solvent was evaporated under reduced pressure. The residue was purified by flash column chromatography on silica gel, eluting with hexane/ethyl acetate, to give the title compound as a colorless oil (108.03 g), containing 11% unreacted 2-benzyloxy-5-(trifluoromethoxy)iodobenzene. 1H NMR (360 MHz, CDCl3) δ 7.67 (1H, d, J=2.8 Hz), 7.40 (5H, m), 7.16 (1H, dd, J=8.9, 2.8 Hz), 6.82 (1H, d, J=8.9 Hz), and 5.14 (2H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06613765B1 |
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| Source dataset | uspto-grants-2003_09 |
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| ORD ID | ord-a0c13e8ec4394029be7a63e6858c7187 |
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| Source note | uspto-grants-2003_09 |
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