HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → 4-Fluoro-N-[3-(1H-imidazol-1-yl)propyl]benzeneacetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 2-(4-Fluorophenyl)acetic acid | HCID 9837 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | 3-(Imidazole-1-yl)-propylamine Dihydrochloride | HCID 12250969 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Fluoro-N-[3-(1H-imidazol-1-yl)propyl]benzeneacetamide | HCID 13588955 | — |
Reaction Steps
A mixture of 1.54 g. of 4-fluorophenylacetic acid, 1.62 g. of 1,1'-carbonyldiimidazole and 30 ml. of tetrahydrofuran was stirred for 2 hours, then 1.98 g. of 1H-imidazole-1-propanamine dihydrochloride was added. Stirring was continued at room temperature for an additional 18 hours, then 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 volatile material. The residue was diluted with methylene chloride and 25 ml. of 1N sodium hydroxide and the layers separated. The organic layer was washed with water, dried over magnesium sulfate and concentrated, giving the desired product as a viscous oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04568687 |
| Source dataset | uspto-grants-1986_02 |
| ORD ID | ord-10943a0c07ab4282b49f50323488230c |
| Source note | uspto-grants-1986_02 |