HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → 2-Phenyl-3-[3(N-methylpiperazino)propionyl]benzofuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Tetrafluoro-m-phenylenediamine dihydrochloride | HCID 149026 | — |
| Reactant | 1-Methylpiperazine dihydrochloride | HCID 2734715 | — |
| Reactant | 1-(2-Phenylbenzofuran-3-yl)ethanone | HCID 13024726 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 2-Phenyl-3-[3(N-methylpiperazino)propionyl]benzofuran | HCID 21452746 | — |
Reaction Steps
To a solution of 23.6 grams of 2-phenyl-3-acetylbenzofuran in 100 milliliters of isopropanol were added 4.2 grams of paraformaldehyde and 19.1 grams of N-methylpiperazine dihydrochloride and the mixture was heated under gentle reflux for a period of 12 hours. The dihydrochloride of the compound named in the heading of this example precipitated from the reaction mixture and was separated therefrom by suction filtration, washed with a small quantity of ethanol, and recrystallized from ethanol. The dihydrochloride had a melting point of 174°-177°C and 22.8 grams thereof was thus obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04009184 |
| Source dataset | uspto-grants-1977_02 |
| ORD ID | ord-6802c8bf4a2c4fd38383ba23faa78f69 |
| Source note | uspto-grants-1977_02 |