HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1183750Generated: November 1, 2026
HCID 57995663, compound → HCID 68733665, compound
https://huagongshe.com/reaction/1183750
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 57995663 | HCID 57995663 | — |
| Reactant | HCID 178418546 | HCID 178418546 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | HCID 68733665 | HCID 68733665 | 60.9% |
Reaction Steps
To a stirred solution of ethyl 2-(6-(cyclopropylmethoxy)-5-iodo-4′-(trifluoromethyl)biphenyl-3-yl)-4-methylpentanoate (0.25 g, 0.447 mmol) in NMP (10 mL) was added CuCN (50 mg, 0.536 mmol) at RT under inert atmosphere. The reaction mixture was stirred at 200° C. temperature over a period of 2 h. After completion of starting material (by TLC), the reaction mixture was cooled to RT and extracted with EtOAc (3×20 mL). Combined organic layers were washed with water (3×15 mL), brine and dried over Na2SO4. After filtration and evaporation, the crude material was purified by column chromatography to afford ethyl 2-(5-cyano-6-(cyclopropylmethoxy)-4′-(trifluoromethyl)biphenyl-3-yl)-4-methylpentanoate (0.125 g) a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08664249B2 |
|---|
| Source dataset | uspto-grants-2014_03 |
|---|
| ORD ID | ord-9239a2e6e35740da9f2c0147f3513d28 |
|---|
| Source note | uspto-grants-2014_03 |
|---|