Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | 2-Phenoxybenzoyl chloride | HCID 11075303 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 3402305 | HCID 3402305 | — |
Reaction Steps
7.7 parts of 2-phenoxybenzoyl chloride was added dropwise to a solution of 2.5 parts of pyrrolidine in 20 parts of pyridine at 0°. When the addition was complete the mixture was stirred for 5 hours. The temperature was then allowed to rise to room temperature and the reaction mixture was poured into 100 parts of water. The aqueous solution was then extracted with chloroform, and washed with water. The chloroform layer was dried over magnesium sulfate, removal of the magnesium sulfate by filtration and concentration of the filtrate gave 6.4 parts of N-(2-phenoxybenzoyl)pyrrolidine, NMR (CDCl3) 1.8δ(m,4H,CH2), 3.4δ(m,4H-N-CH2), 7.1δ(m,9H,Aromatic H). The following compounds can be prepared from the 2-substituted benzoyl chloride and the appropriate secondary amine as described above.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04208205 |
|---|
| Source dataset | uspto-grants-1980_06 |
|---|
| ORD ID | ord-02e3141ad9d74baead51f93f9cf6ccb0 |
|---|
| Source note | uspto-grants-1980_06 |
|---|