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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1274450Generated: November 1, 2026

1-Chloro-3-iodopropane → Ethyl 4-(3-chloropropyl)-4-cyano-1-piperidinecarboxylate

https://huagongshe.com/reaction/1274450

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloro-3-iodopropaneHCID 81363—
ReactantLithium diisopropylamideHCID 2724682—
ReactantEthyl 4-cyanopiperidine-1-carboxylateHCID 4060541—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 4-(3-chloropropyl)-4-cyano-1-piperidinecarboxylateHCID 983804464.6%

Reaction Conditions

Temperature-10 °C

Reaction Steps

To a solution of ethyl 4-cyano-1-piperidinecarboxylate (6.0 g) in tetrahydrofuran (120 ml) at -70° C., under nitrogen, was added a solution of lithium diisopropylamide (4.6 g) in tetrahydrofuran (21.5 ml), dropwise, with stirring. The reaction was allowed to warm to -10° C. and after 30 min was recooled to -70° C. A solution of 1-chloro-3-iodopropane (7.4 g) in tetrahydrofuran (20 ml) was added to the mixture over 30 min. The reaction mixture was quenched with water and allowed to warm to ambient temperature. The mixture was extracted with ethyl acetate. The extracts were washed with water, saturated sodium chloride solution, dried over anhydrous magnesium sulfate and filtered. The filtrate was concentrated in vacuo and the residue was flash chromatographed (silica), eluting with 2:1 heptane/ethyl acetate. The appropriate fractions were collected and concentrated to afford 5.5 g (64%) of product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06156901
Source datasetuspto-grants-2000_12
ORD IDord-4244c3308c8b458fae2491019ac2674d
Source noteuspto-grants-2000_12