HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyanogen Bromide → {2-[1-(4-Methoxyphenyl)cyclopentyl]ethyl}methylcyanamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyanogen Bromide | HCID 10476 | — |
| Reactant | HCID 20364029 | HCID 20364029 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | {2-[1-(4-Methoxyphenyl)cyclopentyl]ethyl}methylcyanamide | HCID 53992609 | — |
Reaction Steps
By following the manipulative procedure outlined above in Example 12, a solution of 5.43 g of 1-(2-dimethylaminoethyl)-1-(4-methoxyphenyl)cyclopentane (the free base of Example 46) in chloroform is added to a stirred solution of 2.57 g of cyanogen bromide in chloroform to give an oil. The oil is dissolved in chlorofrom, subjected to column chromatography with a silica gel column and eluted with ether to produce an orange oil of 1-(N-cyano-N-methylaminoethyl)-1-(4-methoxyphenyl)cyclopentane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04079141 |
| Source dataset | uspto-grants-1978_03 |
| ORD ID | ord-631257f9d82d4b87accfa6817a16f9d0 |
| Source note | uspto-grants-1978_03 |