HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formamide → HCID 57188869, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formamide | HCID 713 | — |
| Reactant | 6-Phenylhexan-3-one | HCID 100910 | — |
| Solvent | Formic Acid | HCID 284 | — |
| Product | HCID 57188869 | HCID 57188869 | — |
Reaction Steps
Ethyl magnesium bromide was reacted with 4-phenylbutylnitrile to provide ethyl 3-phenylpropyl ketone. The ketone was reacted with formamide and formic acid to afford 1-ethyl-4-phenylbutylamine. Methylation of the amine by reaction with formaldehyde and formic acid provided N,N-dimethyl-1-ethyl-4-phenylbutylamine. Quaternization of 6.2 g. of the dimethylamine according to the procedure of Example 62 afforded 6.56 g. of N,N,N-Trimethyl-1-ethyl-4-phenylbutylammonium bromide. M.P. 183°-185° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04395410 |
| Source dataset | uspto-grants-1983_07 |
| ORD ID | ord-ccda9c2d095f444e93afaf0502549b69 |
| Source note | uspto-grants-1983_07 |