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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 390325Erstellt: 24. Oktober 2026

Water → tert-Butyl 4-cyano-4-methylpiperidine-1-carboxylate

https://huagongshe.com/de/reaction/390325

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktMethyl iodideHCID 6328—
EduktTert-butyl 4-cyanopiperidine-1-carboxylateHCID 1514443—
EduktLithium HexamethyldisilazideHCID 2733832—
LösungsmittelTetrahydrofuranHCID 8028—
Produkttert-Butyl 4-cyano-4-methylpiperidine-1-carboxylateHCID 46835621—

Reaktionsschritte

To a solution of tert-butyl 4-cyanopiperidine-1-carboxylate (0.500 g, 2.38 mmol) in 15 mL of THF at −78° C. was added lithium bis(trimethylsilyl)amide (1 M solution in diethyl ether, 5.23 mL, 5.23 mmol). After 20 min, iodomethane (0.338 g, 2.38 mmol) was added dropwise, and the reaction was slowly warmed to rt. After 15 h, the mixture was cooled to 0° C., treated with water, and extracted 3× with ethyl acetate. The solution was extracted 3× with ethyl acetate, and the combined organic solution was washed with water and brine, dried over sodium sulfate, filtered, and concentrated in vacuo to provide tert-butyl 4-cyano-4-methylpiperidine-1-carboxylate that gave a proton NMR spectra consistent with theory.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08383638B2
Quelldatensatzuspto-grants-2013_02
ORD IDord-454eebe664044bada4195fc24971f482
Quellennotizuspto-grants-2013_02