HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → 1-(Piperidin-1-yl)-4-(2-fluoro-5-bromobenzyloxy)butane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | HCID 21196139 | HCID 21196139 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(Piperidin-1-yl)-4-(2-fluoro-5-bromobenzyloxy)butane | HCID 21196109 | — |
Reaction Steps
A solution of 4-(2-fluoro-5-bromobenzyloxy)butyl bromide (520 mg, 1.53 mmol) in tetrahydrofuran (8 ml) was treated with piperidine (1.5 ml, 15.3 mmol). The resulting reaction mixture was stirred for about 24 hours. The reaction mixture was then diluted with methylene chloride and washed with saturated sodium bicarbonate. The organic fraction was dried over sodium sulfate and the solvents were removed in vacuo. The desired title intermediate was further purified by radial chromatography.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06245761B1 |
| Source dataset | uspto-grants-2001_06 |
| ORD ID | ord-ea1c3d25f6f8406f9103a277347bf27b |
| Source note | uspto-grants-2001_06 |