HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → N-[3-(1H-imidazol-1-yl)propyl]-2-phenoxyacetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Phenoxyacetic Acid | HCID 19188 | — |
| 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]-2-phenoxyacetamide | HCID 5081968 | — |
Reaction Steps
A mixture of 2.28 g. of phenoxyacetic acid, 2.43 g. of 1,1'-carbonyldiimidazole and 50 ml. of tetrahydrofuran was stirred at room temperature for 2 hours, then 3.0 g. of 1H-imidazole-1-propanamine dihydrochloride was added. The reaction mixture was stirred for 18 hours, then heated at reflux temperature for 5 hours, 5 ml. of water was added, the mixture was heated for 30 minutes and then concentrated to remove the tetrahydrofuran. The residue was treated with methylene chloride and 50 ml. of 1N sodium hydroxide and the layers separated. The organic layer was washed with water, dried over magnesium sulfate and concentrated. The residue was washed onto a filter with ether, giving the desired product, m.p. 91°-93° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04568687 |
| Source dataset | uspto-grants-1986_02 |
| ORD ID | ord-de6934bdb7514aa2bab718b2e63cf2d8 |
| Source note | uspto-grants-1986_02 |