HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → 1-(4-Iodobenzyl)piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-Iodobenzyl bromide | HCID 954258 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(4-Iodobenzyl)piperidine | HCID 7537600 | 99.6% |
Reaction Steps
To a mixture of 0.31 g of piperidine (3.6 mmol) and 0.47 g of N,N-diisopropylethylamine 3.6 mmol) in 10 mL of dichloromethane was added 0.90 g of 4-iodobenzylbromide (3 mmol). The mixture was allowed to stir for 16 h and partitioned between 50 mL of EtOAc and 50 mL of water. The layers were separated and the EtOAc was washed with 25 mL of brine, dried (MgSO4) and concentrated in vacuo to give 0.90 g of 4-(N-piperidinylmethyl)iodobenzene. The product was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07405230B2 |
| Source dataset | uspto-grants-2008_07 |
| ORD ID | ord-59030196d9cc42f38bf449ac9db20efa |
| Source note | uspto-grants-2008_07 |