HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl bromoacetate → HCID 20375653, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | 3-Phenoxypyridine | HCID 200510 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 20375653 | HCID 20375653 | — |
Reaction Steps
To a solution of 17.1 g of 3-phenoxypyridine [J. Amer. Chem. Soc 59, 297 (1937)] in 100 ml of acetonitrile is added 16.7 g of ethyl bromoacetate and the solution is refluxed for 8 hours. The resulting mixture is concentrated at reduced pressure and the crystalline solid is isolated by filtration to yield 1-(2-ethoxy-2-oxoethyl)-3-phenoxypyridinium bromide; mp 125°-126° C. after recrystallization from acetonitrile-diethyl ether.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04187311 |
| Source dataset | uspto-grants-1980_02 |
| ORD ID | ord-29ebd4fa5934430da8258585cd8ffab2 |
| Source note | uspto-grants-1980_02 |