HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 355461Generated: October 28, 2026
Diethyl Ether → 1,4-Dibenzyl-4-cyanopiperidine
https://huagongshe.com/reaction/355461
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 4-Cyanopiperidine | HCID 138223 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Solvent | Cyclohexane | HCID 8078 | — |
| Product | 1,4-Dibenzyl-4-cyanopiperidine | HCID 22741742 | — |
Reaction Steps
A solution of 15 g of 4-cyanopiperidine in 250 ml of THF is cooled to -50° C., 190 ml of a 1.5M solution of lithium diisopropylamide in cyclohexane is added dropwise and the mixture is left stirring for 30 minutes at -50° C. 34 ml of benzylbromide are then added slowly and the mixture is left stirring for 3 hours while allowing the temperature to rise to RT. The reaction mixture is poured into an ice/concentrated HCl mixture, ether is added and the precipitate formed is drained and washed with water. The precipitate is taken up in water, the mixture is alkalinized to pH 12 by adding concentrated NaOH solution and extracted with ether, the organic phase is dried over MgSO4 and the solvent is evaporated off under vacuum. 31.7 g of the expected product are obtained after crystallization in pentane, m.p.=92° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05830906 |
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| Source dataset | uspto-grants-1998_11 |
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| ORD ID | ord-02964c1ce5dc440b8b560165e012ed90 |
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| Source note | uspto-grants-1998_11 |
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