HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → 1-{4-[(4-cyanobenzyl)oxy]phenyl}-1H-indole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Tris(hydroxymethyl)aminomethane | HCID 6503 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-(Bromomethyl)benzonitrile | HCID 86996 | — |
| Reactant | 1-(4-hydroxyphenyl)-1H-indole | HCID 16655672 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-{4-[(4-cyanobenzyl)oxy]phenyl}-1H-indole | HCID 68545969 | 77.1% |
Reaction Steps
To a solution of 0.038 g (0.18 mmol) 1-(4-hydroxyphenyl)-1H-indole in 1.2 ml DMF was added 0.05 g (0.38 mmol) K2CO3 and the slurry was mixed for 30 min. 59 mg (0.3 mmol) α-bromo-p-tolunitrile and 0.01 g (66 μmol) NaI was added and the slurry was mixed at 60° C. for 4 hr. The solution was allowed to cool and an additional 2 ml DMF was added, followed by 0.10 g PS-Trisamine scavenger reagent (Argonaut Technologies, San Carlos, Calif.). The slurry was mixed at 60° C. for a further 3 hr and allowed to cool. The reaction was filtered and the solution was concentrated to afford 0.045 g 1-{4-[(4-cyanobenzyl)oxy]phenyl}-1H-indole as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07259182B2 |
| Source dataset | uspto-grants-2007_08 |
| ORD ID | ord-a1d918ed61064565b675a62c7ff35f08 |
| Source note | uspto-grants-2007_08 |