HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1015934Generated: October 31, 2026
Potassium Carbonate → Methyl 4-[(4E)-5-(5-fluoro-2-{[4-(trifluoromethyl)benzyl]oxy}phenyl)-3-{2-[4-(methoxycarbon-yl)phenyl]ethyl}pent-4-en-1-yl]benzoate
https://huagongshe.com/reaction/1015934
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-(Bromomethyl)-4-(trifluoromethyl)benzene | HCID 123062 | — |
| Reactant | Methyl 4-[(4E)-5-(5-fluoro-2-hydroxyphenyl)-3-{2-[4-(methoxycarbonyl)phenyl]ethyl}pent-4-en-1-yl]benzoate | HCID 59397498 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Methyl 4-[(4E)-5-(5-fluoro-2-{[4-(trifluoromethyl)benzyl]oxy}phenyl)-3-{2-[4-(methoxycarbon-yl)phenyl]ethyl}pent-4-en-1-yl]benzoate | HCID 59397499 | — |
Reaction Steps
280 mg (1.2 mmol) of 1-(bromomethyl)-4-(trifluoromethyl)benzene and 162 mg (1.2 mmol) of anhydrous potassium carbonate are added to a solution of 279 mg (0.59 mmol) of methyl 4-[(4E)-5-(5-fluoro-2-hydroxyphenyl)-3-{2-[4-(methoxycarbonyl)phenyl]ethyl} pent-4-en-1-yl]benzoate in 6.5 ml of dry acetonitrile, and the mixture is then heated at 60° C. for 12 hours. The mixture is then filtered, and the filtrate is evaporated to dryness. The residue is purified by preparative HPLC. This gives 274 mg (0.43 mmol, 74% of theory) of a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07985876B2 |
|---|
| Source dataset | uspto-grants-2011_07 |
|---|
| ORD ID | ord-1119bf46909c46fcb28a6e815541bf01 |
|---|
| Source note | uspto-grants-2011_07 |
|---|