HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoic Acid → N-[3-(1H-imidazol-1-yl)propyl]benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoic Acid | HCID 243 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | 3-(Imidazole-1-yl)-propylamine Dihydrochloride | HCID 12250969 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-[3-(1H-imidazol-1-yl)propyl]benzamide | HCID 3584880 | — |
Reaction Steps
A mixture of 1.22 g. of benzoic acid, 1.62 g. of 1,1'-carbonyldiimidazole and 30 ml. of tetrahydrofuran was stirred for 3 hours, then 1.98 g. of 1H-imidazole-1-propanamine dihydrochloride was added. The reaction mixture was stirred for 18 hours, then heated at reflux for 5 hours, then diluted with 5 ml. of water and heated for an additional 30 minutes. The mixture was concentrated to remove most of the solvent and to the residue was added chloroform and 35 ml. of 1N sodium hydroxide. The layers were separated. The organic layer was washed with water, dried over magnesium sulfate, concentrated and diethyl ether was added, giving the desired product, m.p. 134°-136° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04568687 |
| Source dataset | uspto-grants-1986_02 |
| ORD ID | ord-2e1c3b8836f5483abd58430c707b46a2 |
| Source note | uspto-grants-1986_02 |