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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1869463Generated: October 30, 2026

Methyl iodide → tert-Butyl 4-cyano-4-methylpiperidine-1-carboxylate

https://huagongshe.com/reaction/1869463

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantTert-butyl 4-cyanopiperidine-1-carboxylateHCID 1514443—
ReactantLithium HexamethyldisilazideHCID 2733832—
SolventTetrahydrofuranHCID 8028—
Producttert-Butyl 4-cyano-4-methylpiperidine-1-carboxylateHCID 46835621—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 4-cyano-piperidine-1-carboxylic acid tert-butyl ester (4.52 g, 20 mmol) in THF (50 mL) was added LHMDS in THF (24 mL, 24 mmol) at 0° C. After stirring at 0° C. for 1 hour, MeI (5.7 g) was added. The reaction mixture was kept at 0° C. for 2 hours, then partitioned between EtOAc and H2O. After concentration in vacuo, the residue was purified by silica column chromatography with EtOAc/hexanes to give the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07638541B2
Source datasetuspto-grants-2009_12
ORD IDord-9281bceadf32437483d70449f4b507d9
Source noteuspto-grants-2009_12