HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 446Generated: October 24, 2026
3-Iodobenzyloxybenzene → 2-Methyl-1-(3-phenylmethoxyphenyl)-6-(trifluoromethoxy)indole
https://huagongshe.com/en/reaction/446
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Iodobenzyloxybenzene | HCID 4228019 | — |
| Reactant | 2-Methyl-6-(trifluoromethoxy)-1H-indole | HCID 12180669 | — |
| Reagent | Sodium t-butoxide | HCID 23676156 | — |
| Catalyst | 2-(Di-tert-butylphosphino)biphenyl | HCID 2734215 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-Methyl-1-(3-phenylmethoxyphenyl)-6-(trifluoromethoxy)indole | HCID 59216720 | 10.45% |
Reaction Steps
EN04773-52, _Buchwald coupling, toluene and iodide_ The indole from 4773-25, 1-(benzyloxy)-3-iodobenzene,Pd2(dba)3, JohnPhos and KOtBu were dissolved in toluene. The mixture was warmed at 120 °C for 1h and 50% conversion was observed on NMR*(see attached NMR). The mixture was warmed further 15h at 120°C, still starting material left but the reaction mixture was directly applied to a silica column (heptane 3:1). Product was collected in fraction 22-23 (see attached NMR). Only 19.3 mg (10.45% yield) could be collected but NMR showed correct product. Test reaction with bromide was performed in 4773-53. ######################### *Small amount from reaction mixture was dissolved in CDCl3 and 1HNMR analysis was performed)
Provenance & Evidence
| Source dataset | 750 AstraZeneca ELN dataset |
|---|
| ORD ID | ord-055c0d9926684c29963cad751105f26e |
|---|
| Source note | 750 AstraZeneca ELN dataset |
|---|