HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrazine hydrate (1:1) → Ethyl 2-(4-aminobutyl)benzofuran-6-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | Ethyl 2-(4-phthalimidobutyl)benzofuran-6-carboxylate | HCID 20303948 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 2-(4-aminobutyl)benzofuran-6-carboxylate | HCID 20303943 | — |
Reaction Steps
A solution of ethyl 2-(4-phthalimidobutyl)-benzofuran-6-carboxylate (3.9 g., 0.01 mole) and hydrazine hydrate (0.55 g., 0.011 mole) in ethanol (20 ml.) is heated at 60° C. for 8 hours. The solvent is evaporated at reduced pressure. The solid residue is treated with water and 5 N sodium hydroxide solution and then is extracted with chloroform. The evaporation of the solvent from the organic extract provides ethyl 2-(4-aminobutyl)benzofuran-6-carboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04238487 |
| Source dataset | uspto-grants-1980_12 |
| ORD ID | ord-d922f6130deb42128e2a017f0f1b438c |
| Source note | uspto-grants-1980_12 |