HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → N-(4-chlorophenyl)-1-(2-propenyl)-4-piperidinamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N-(4-chlorophenyl)piperidin-4-amine | HCID 7183033 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | N-(4-chlorophenyl)-1-(2-propenyl)-4-piperidinamine | HCID 23339007 | — |
Reaction Steps
To a stirred mixture of 15 parts of N-(4-chlorophenyl)-4-piperidinamine, 12 parts of N,N-diethylethanamine in 130 parts of benzene is added dropwise a solution of 10.3 parts of 3-bromo-1-propene in 70 parts of benzene. Upon completion, the whole is stirred first for 20h. 30 at room temperature and further for 40 minutes at reflux. The reaction mixture is cooled, filtered and the filtrate is evaporated. The residue is taken up in 1,1'-oxybisethane and treated with activated charcoal. The latter is filtered off and the 1,1'-oxybisethane is evaporated again, yielding 2.9 parts of N-(4-chlorophenyl)-1-(2-propenyl)-4-piperidinamine; mp. 90° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04126689 |
| Source dataset | uspto-grants-1978_11 |
| ORD ID | ord-1f6bf37f4aa04adb933352b15139e5b7 |
| Source note | uspto-grants-1978_11 |