Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromomethylcyclopropaneHCID 81503—
ReactantTert-butyl 4-cyanopiperidine-1-carboxylateHCID 1514443—
ReactantLithium diisopropylamideHCID 2724682—
SolventTetrahydrofuranHCID 8028—
SolventSodium chloride; waterHCID 57417360—
ProductTert-butyl 4-cyano-4-(cyclopropylmethyl)piperidine-1-carboxylateHCID 57425738—

Reaction Conditions

Temperature-70 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07655644B2
Source datasetuspto-grants-2010_02
ORD IDord-6fbb7f74cc6f4b4685783b53b9325fbd
Source noteuspto-grants-2010_02