HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Iodo-1-tritylimidazole → (4-Cyano-3-fluorophenyl)[1-(triphenylmethyl)imidazol-4-yl]methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Iodo-1-tritylimidazole | HCID 618252 | — |
| Reactant | 2-Fluoro-4-formylbenzonitrile | HCID 11217339 | — |
| Reactant | HCID 178418443 | HCID 178418443 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (4-Cyano-3-fluorophenyl)[1-(triphenylmethyl)imidazol-4-yl]methanol | HCID 11134299 | — |
Reaction Conditions
| Temperature | -78 °C |
|---|
Reaction Steps
To a solution of 4-iodo-1-trityl-1H-imidazole (5.00 g, 11.5 mmol) in anhydrous CH2Cl2 (30 mL) was added a 3.0M solution of ethylmagnesium bromide (6.58 mL, 19.7 mmol) with stirring under Ar. After 3 h, the reaction mixture was cooled to −78° C. and a solution of 2-fluoro-4-formyl-benzonitrile (as described in Step A above) (1.70 g, 11.5 mmol) dissolved in CH2Cl2 (20 mL) was added dropwise. The reaction was allowed to warm to RT over 2 h, quenched with saturated NH4Cl solution, diluted with satd. NaHCO3 solution to pH=8.5, and extracted with CH2Cl2 (3×). The combined organic layers were dried (MgSO4), concentrated and purified using SiO2 chromatography (0-1% MeOH/CH2Cl2) to yield the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06284755B1 |
| Source dataset | uspto-grants-2001_09 |
| ORD ID | ord-d78255479d3345df96a0146c8a8c0251 |
| Source note | uspto-grants-2001_09 |