HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl bromoacetate → 1,2-Di-[(ethoxycarbonyl)methyl]pyridinium bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Ethyl 2-pyridylacetate | HCID 75960 | — |
| Product | 1,2-Di-[(ethoxycarbonyl)methyl]pyridinium bromide | HCID 21467252 | 30% |
Reaction Steps
A mixture of ethyl 2-pyridylacetate (6.0 g, 0.036 mole) and ethyl bromoacetate (4.4 ml, 0.038 mole) was allowed to stand at room temperature for 72 h, during which time the product gradually crystallised out. The mixture was treated with acetone (80 ml) to dissolve unreacted starting materials and then filtered. The solid collected was dried under vacuum to afford 1,2-di-[(ethoxycarbonyl)methyl]pyridinium bromide as a beige solid (3.53 g, 30%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05696129 |
| Source dataset | uspto-grants-1997_12 |
| ORD ID | ord-1e0d0fffc70c4cc094f4313a5d7738d0 |
| Source note | uspto-grants-1997_12 |