HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Bromide → 2-Bromo-5-ethoxypyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Bromide | HCID 6332 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Bromo-5-hydroxypyridine | HCID 2762865 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-Bromo-5-ethoxypyridine | HCID 23436892 | — |
Reaction Steps
2.51 g (22.99 mmol) 1-bromoethane and 1.99 g (14.37 mmol) K2CO3 are added to a mixture of 1.0 g (5.75 mmol) 2-bromo-5-hydroxypyridine in 100 mL ACN. The mixture is stirred at reflux over night. Then the reaction mixture is poured onto water and extracted with TBME. The organic layer is dried with Na2SO4 and the solvent is removed under vacuo. The residue is purified by column chromatography (silica gel, PE/EtOAC 1/1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08530460B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-52b68b2543574d2f8bafa4e5182d8539 |
| Source note | uspto-grants-2013_09 |