HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → Ethyl 3-(2-chloropyridin-5-yl)propionate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | (E)-Ethyl 3-(6-chloropyridin-3-YL)acrylate | HCID 53406713 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 3-(2-chloropyridin-5-yl)propionate | HCID 19082020 | 84% |
Reaction Steps
A suspension of 0.84 g (1 eq) of Te powder and 0.6 g (2 eq) of NaBH4 in 32 ml of ethanol was heated under nitrogen until it became a homogeneous purple solution. To the above hot solution was added ethyl β-(2-chloropyridin-5yl)acrylate (1.38 g, 6.5 mmol) and the mixture was refluxed for 4 h. The crude product was purified by flash chromatography (silica gel; hexane/ethyl acetate, 3:1) to afford 1.11 g (84,6%) of ethyl 3-(2-chloropyridin-5-yl)propionate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05618821 |
| Source dataset | uspto-grants-1997_04 |
| ORD ID | ord-ec542c1c9b2a40199ac51be469a0f6be |
| Source note | uspto-grants-1997_04 |