HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → HCID 13232127, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | 2-(3,5-Dimethylphenoxy)butanoyl chloride | HCID 13232126 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 13232127 | HCID 13232127 | 62.1% |
Reaction Steps
In 30 ml of benzene were dissolved 1.8 g (0.017 mole) of benzylamine and 1.2 g (0.015 mole) of pyridine, and thereto was added dropwise 3.0 g (0.013 mole) of 2-(3,5-dimethylphenoxy)-butyroyl chloride at room temperature with stirring. After the reaction was carried out for 5 hours, the reaction mixture was washed with water, dilute hydrochloric acid, dilute aqueous sodium hydroxide and then water successively. After the benzene layer was dried, the benzene was removed by distillation. The resultant crude crystals were recrystallized from n-hexane to give 2.4 g of N-benzyl-2-(3,5-dimethylphenoxy)-butyramide melting at 93°-94° C. as colorless needles.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04753674 |
| Source dataset | uspto-grants-1988_06 |
| ORD ID | ord-5c6aea464da4439da909422d134aaa9b |
| Source note | uspto-grants-1988_06 |