HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethylamine → ethyl 5-(N,N-diethylaminomethyl)-2-furoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethylamine | HCID 8021 | — |
| Reactant | Ethyl 5-(chloromethyl)-2-furancarboxylate | HCID 263166 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | ethyl 5-(N,N-diethylaminomethyl)-2-furoate | HCID 20346154 | — |
Reaction Steps
Ethyl 5-(chloromethyl)-2-furoate (0.1 mole) is refluxed with diethylamine (0.25 mole) in 40 ml of benzene for one hour. The benzene solution is filtered off and washed with water. The organic layer is separated and dried over magnesium sulfate. The magnesium sulfate is removed by filtration and the organics are evaporated to dryness. The residue is distilled to give a pure fraction of ethyl 5-(N,N-diethylaminomethyl)-2-furoate boiling at 97°-106° C. at 0.1 mm of Hg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04195023 |
| Source dataset | uspto-grants-1980_03 |
| ORD ID | ord-3dc60f99f2a140ba89ca3e4738118d19 |
| Source note | uspto-grants-1980_03 |