HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 453558Generated: October 31, 2026
Potassium Carbonate → Tert-butyl 2-(4-(4-((2,4-dichlorophenethyl)carbamoyl)-3-fluorophenoxy)-3-cyanophenyl)acetate
https://huagongshe.com/reaction/453558
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Tert-butyl 2-(3-cyano-4-fluorophenyl)acetate | HCID 45925946 | — |
| Reactant | N-(2,4-dichlorophenethyl)-2-fluoro-4-hydroxybenzamide | HCID 68467622 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Tert-butyl 2-(4-(4-((2,4-dichlorophenethyl)carbamoyl)-3-fluorophenoxy)-3-cyanophenyl)acetate | HCID 68468374 | 2.3% |
Reaction Steps
To a stirred solution of N-(2,4-dichlorophenethyl)-2-fluoro-4-hydroxybenzamide (420 mg, 1.28 mmol) and tert-butyl 2-(3-cyano-4-fluorophenyl)acetate (361 mg, 1.54 mmol) in DMSO (6 ml) was added K2CO3 (265 mg, 1.92 mmol). The reaction was heated stirred at 70° C. for one hour. The reaction was then stirred at 90° C. overnight. The reaction was diluted with water and ethyl acetate. The aqueous phase was extracted with ethyl acetate and the combined organic layers were washed with 10% Na2CO3 and brine, dried over MgSO4, filtered and concentrated. The crude product was purified by silica gel chromatography to give tert-butyl 2-(4-(4-((2,4-dichlorophenethyl)carbamoyl)-3-fluorophenoxy)-3-cyanophenyl)acetate (0.0157 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08492437B2 |
|---|
| Source dataset | uspto-grants-2013_07 |
|---|
| ORD ID | ord-ba8b5d0c23ec4259831d252e8cf9dedf |
|---|
| Source note | uspto-grants-2013_07 |
|---|