HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2-Chloroacetyl-1-(o-fluorophenethyl)pyrrole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Chloroacetonitrile | HCID 7856 | — |
| Reactant | 1-[(2-Fluorophenyl)methyl]-1H-pyrrole | HCID 14391472 | — |
| Reactant | 2-Chloro-1-{1-[(2-fluorophenyl)methyl]-1H-pyrrol-2-yl}ethan-1-one | HCID 20391531 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-Chloroacetyl-1-(o-fluorophenethyl)pyrrole | HCID 20391533 | — |
| Product | o-Fluorophenethylpyrrole | HCID 54477722 | — |
Reaction Steps
A solution of 40 g of 1-(o-fluorobenzyl)pyrrole and 17.2 g of chloroacetonitrile in 200 ml of anhydrous ether at a temperature between 0 and -5° C is saturated with hydrogen chloride gas and then the solution is stirred until a heavy white cake forms. This cake is broken up and permitted to sit for one hour at ambient temperature. The white solid is filtered, washed with ether and dried and then hydrolyzed in water and extracted with ether. Concentration of the ether extracts leaves white crystals, mp 76°-78° C, of 2-chloroacetyl-1-(o-fluorobenzyl)pyrrole. The analagous treatment of o-fluorophenethylpyrrole produces 2-chloroacetyl-1-(o-fluorophenethyl)pyrrole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04107074 |
| Source dataset | uspto-grants-1978_08 |
| ORD ID | ord-88f92307f7b442dba23215e5c8fe6f63 |
| Source note | uspto-grants-1978_08 |