HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → (5-Bromopentyl)cyclohexane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Phosphorus tribromide | HCID 24614 | — |
| Reactant | Cyclohexanepentanol | HCID 269450 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (5-Bromopentyl)cyclohexane | HCID 14952366 | — |
Reaction Steps
To a stirred solution of 5-cyclohexylpentanol (1.74 g., 10.25 mmol) and pyridine (0.94 g., 11.1 mmol) at 0° under argon was added phosphorus tribromide (1.21 g., 4.5 mmol) dropwise. The reaction mixture became viscous, therefore 25 ml tetrahydrofuran was added. This mixture was stirred for 1.5 hours at room temperature, then partitioned between ethyl ether and 5% aqueous hydrochloric acid. The organic portion was washed with a 5% sodium bicarbonate solution, water, saturated sodium chloride solution, dried over magnesium sulfate, filtered and concentrated to give a dark yellow oil. Purification by flash chromatography (silica, hexane) yielded the desired alkyl halide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05134128 |
| Source dataset | uspto-grants-1992_07 |
| ORD ID | ord-93b334b57cf84c8e8dca500a087d273c |
| Source note | uspto-grants-1992_07 |