HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Methylaniline → Ethyl 5-[methyl(phenyl)amino]pentanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Methylaniline | HCID 7515 | — |
| Reactant | 2,6-Lutidine | HCID 7937 | — |
| Reactant | HCID 22174073 | HCID 22174073 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Ethyl 5-[methyl(phenyl)amino]pentanoate | HCID 19438629 | — |
Reaction Steps
5.52 ml (48 mmol) of N-Methyl aniline, 8 ml Bromovalerate (50.2 mmol) and 2,6-lutidine (5.82 ml, 50.2 mmol) were taken in 100 ml acetonitrile and the reaction was refluxed for 24 hour under stirring. Acetonitrile was removed under vacuum and residues were dissolved in ether. The organic phase was washed with water. After drying over magnesium sulfate and filtering, the solvent was removed to give a brown liquid. The residue was purified by flash chromatography on silica gel using a 10% ethyl acetate in hexane as eluent gave 10.1 g light yellow oil as product. MW C14H21NO2 235.32 g/mol (yields 90%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09023998B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-ea4d2a6f980a4bda988e8e7480c2e5de |
| Source note | uspto-grants-2015_05 |