HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,2-Dimethoxyethylmethylamine → ethyl 5-chloro-3-[N-(2,2 dimethoxyethyl)-N methyl(aminomethyl)]-2-benzofurancarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,2-Dimethoxyethylmethylamine | HCID 8503 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl 3-bromomethyl-5-chloro-2-benzofurancarboxylate | HCID 15678689 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | ethyl 5-chloro-3-[N-(2,2 dimethoxyethyl)-N methyl(aminomethyl)]-2-benzofurancarboxylate | HCID 15678690 | — |
Reaction Steps
A mixture of ethyl 3-bromomethyl-5-chloro-2-benzofurancarboxylate (52.75 g, 0.166 mol), methylaminoacetaldehyde dimethyl acetal (19.0 g, 0.167 mol) and potassium carbonate (45 g) in dry acetone (600 ml) was stirred under argon for 30 hours, filtered and the filtrate evaporated. The residue was partitioned between ethyl ether and water and the organic phase was dried with magnesium sulfate, filtered, and concentrated to give ethyl 5-chloro-3-[N-(2,2-dimethoxyethyl)-N-methyl(aminomethyl)]-2-benzofurancarboxylate: mp 58°-60° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04978660 |
| Source dataset | uspto-grants-1990_12 |
| ORD ID | ord-8d38d819b1f043fca57ceec45a2a035a |
| Source note | uspto-grants-1990_12 |