HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1426353Generated: November 4, 2026
Ethyl Acetate → tert-Butyl 4-{[2-(trifluoromethyl)-6-vinylpyrimidin-4-yl]oxy}piperidine-1-carboxylate
https://huagongshe.com/reaction/1426353
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | tert-Butyl 4-{[6-chloro-2-(trifluoromethyl)pyrimidin-4-yl]oxy}piperidine-1-carboxylate | HCID 86666510 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Potassium Fluoride | HCID 522689 | — |
| Product | tert-Butyl 4-{[2-(trifluoromethyl)-6-vinylpyrimidin-4-yl]oxy}piperidine-1-carboxylate | HCID 67954436 | — |
Reaction Steps
To a solution of tert-butyl 4-{[6-chloro-2-(trifluoromethyl)pyrimidin-4-yl]oxy}piperidine-1-carboxylate (0.742 g, 1.94 mmol) in DMF (8.7 mL) was added (2-ethenyl)tri-n-butyltin (0.682 mL, 2.33 mmol) and tetrakis(triphenylphosphine)palladium(0) (112 mg, 0.0972 mmol). The reaction solution was stirred at 65° C. overnight. The reaction solution was diluted with ethyl acetate and saturated KF solution. The aqueous layer was extracted with ethyl acetate three times. The combined organic solutions were dried over Na2SO4, filtered and concentrated. The residue was purified with silica gel column to give the desired product as light brown oil. LCMS (M+H)+: 374.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08933085B2 |
|---|
| Source dataset | uspto-grants-2015_01 |
|---|
| ORD ID | ord-9ce962dae261406a9b526d335a466e24 |
|---|
| Source note | uspto-grants-2015_01 |
|---|