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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1038831Erstellt: 26. Oktober 2026

L-Methionine → Benzyl 4-cyano-4-methylpiperidine-1-carboxylate

https://huagongshe.com/reaction/1038831

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktL-MethionineHCID 6137—
EduktAmmonium ChlorideHCID 25517—
EduktLithium HexamethyldisilazideHCID 2733832—
EduktBenzyl 4-cyanopiperidine-1-carboxylateHCID 22028286—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktBenzyl 4-cyano-4-methylpiperidine-1-carboxylateHCID 6698070680,3%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

LiHMDS (47.6 mL, 47.6 mmol) was added dropwise via syringe to the mixture of benzyl 4-cyanopiperidine-1-carboxylate (8.00 g, 31.8 mmol, [Oakwood]) in THF (50 mL) at about −78° C. and stirred for about 1 h. Met (6.76 g, 47.6 mmol) was added dropwise via syringe at about −78° C. and the mixture was stirred overnight at rt. The solution was cooled to 0° C. and saturated aqueous NH4Cl (200 mL) was added. The mixture was extracted with DCM (3×300 mL). The combined organic extracts were dried over anhydrous Na2SO4, filtered and concentrated in vacuo. The sample was deposited onto silica gel and purified by column chromatography eluting with 10:1 pet ether/EtOAc to give benzyl 4-cyano-4-methylpiperidine-1-carboxylate (6.6 g, 74%): LC/MS (Table 2, Method i) Rt=2.03 min; MS m/z: 259 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08551981B2
Quelldatensatzuspto-grants-2013_10
ORD IDord-636345933a4e4599a0d0118cb39ab536
Quellennotizuspto-grants-2013_10