HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 226392Generated: October 27, 2026
Ethyl Acrylate → Ethyl (E)-3-(2-chloropyrimidin-5-yl)acrylate
https://huagongshe.com/reaction/226392
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acrylate | HCID 8821 | — |
| Reactant | Tri-o-tolylphosphine | HCID 80271 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-Chloro-5-iodopyrimidine | HCID 1714223 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl (E)-3-(2-chloropyrimidin-5-yl)acrylate | HCID 53259409 | — |
Reaction Steps
To a mixture of 2-chloro-5-iodopyrimidine (7.62 g), palladium(II) acetate (356 mg), tri(o-tolyl)phosphine (965 mg), and DMF (32 mL) was added ethyl acrylate (17.2 mL) and N,N-diisopropylethylamine (13.8 mL). After stirring for 3 hours at 100° C., the reaction mixture was partitioned between ethyl acetate and H2O. The organic layer was dried over MgSO4, filtered, and evaporated in vacuo. The residue was purified by column chromatography on silica gel to give ethyl (2E)-3-(2-chloro-5-pyrimidinyl)acrylate (2.32 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07557127B2 |
|---|
| Source dataset | uspto-grants-2009_07 |
|---|
| ORD ID | ord-b212646e797944888b766c08bba54603 |
|---|
| Source note | uspto-grants-2009_07 |
|---|