HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,5-Dibromopentane → 1-(Pyridin-4-yl)cyclohexane-1-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,5-Dibromopentane | HCID 8100 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-Pyridylacetonitrile hydrochloride | HCID 12396608 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-(Pyridin-4-yl)cyclohexane-1-carbonitrile | HCID 22314789 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
A mixture of 3 g of 4-pyridylacetonitrile hydrochloride in 50 ml of DMF is cooled to 0° C., 2.6 g of 60% sodium hydride in oil are added portionwise and the mixture is left stirring at RT for 1 hour 30 minutes. The reaction mixture is cooled on an ice bath, 2.7 ml of 1,5-dibromopentane are added dropwise and this mixture is left stirring at RT for 48 hours. The reaction mixture is poured into saturated NH4CO solution and extracted with ether, the organic phase is washed three times with water and dried over MgSO4, and the solvent is evaporated off under vacuum. The residue is chromatographed on silica H gel, eluting with DCM and, then with a DCM/MeOH mixture (98/2; v/v). 2.5 g of the expected product are obtained; m.p.=79° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06951940B2 |
| Source dataset | uspto-grants-2005_10 |
| ORD ID | ord-e3e4075670234e469b4f20eac236540d |
| Source note | uspto-grants-2005_10 |