HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1441234Generated: November 2, 2026
Bromomethylcyclopropane → Tert-butyl 4-cyano-4-(cyclopropylmethyl)piperidine-1-carboxylate
https://huagongshe.com/reaction/1441234
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromomethylcyclopropane | HCID 81503 | — |
| Reactant | Tert-butyl 4-cyanopiperidine-1-carboxylate | HCID 1514443 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | Tert-butyl 4-cyano-4-(cyclopropylmethyl)piperidine-1-carboxylate | HCID 57425738 | — |
Reaction Steps
To a stirred solution of lithium diisopropylamide (2M solution in THF; 60 ml; 0.12 mol) in THF (60 ml) at −70° C. was added tert-butyl 4-cyanopiperidine-1-carboxylate (21 g; 0.1 mol) in THF (150 ml) over 1 hour. The mixture was stirred at −70° C. for 1 hour and then (bromomethyl)cyclopropane (17.53 g; 0.13 mol) in THF (20 ml) was added. The solution was stirred at −70° C. for 1 hour then allowed to warm to ambient temperature over 2 hours. The reaction was poured into brine (150 ml) and extracted with EtOAc (3×200 ml). The combined organic extracts were washed with brine (200 ml), dried over MgSO4, filtered and evaporated to give a brown oil. The crude product was chromatographed on silica eluted with 5% EtOAc in isohexane to give the title product as a colourless oil. (24.8 g)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07655644B2 |
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| Source dataset | uspto-grants-2010_02 |
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| ORD ID | ord-6fbb7f74cc6f4b4685783b53b9325fbd |
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| Source note | uspto-grants-2010_02 |
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