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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1723841Erstellt: 25. Oktober 2026

Trimethylsilyldiazomethane → 1-tert-Butyl 3-methyl piperidine-1,3-dicarboxylate

https://huagongshe.com/reaction/1723841

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTrimethylsilyldiazomethaneHCID 167693—
Edukt1-((Tert-butoxy)carbonyl)piperidine-3-carboxylic acidHCID 2735647—
LösungsmittelToluene methanolHCID 21867641—
Produkt1-tert-Butyl 3-methyl piperidine-1,3-dicarboxylateHCID 2359065283,7%

Reaktionsschritte

To a room temperature solution of piperidine-1,3-dicarboxylic acid-1-tert-butyl ester (5.00 g, 21.81 mmol) in 20% MeOH/toluene (100 ml) was added 14.18 ml of (trimethylsilyl)diazomethane (2.0 M, 28.35 mmol) dropwise and the reaction was monitored by TLC until completion and then concentrated under reduced pressure to yield 4.44 g (83.7%) of piperidine-1,3-dicarboxylic acid 1-tert-butyl ester-3-methyl ester (Intermediate 53). 1H NMR (400 MHz, CDCl3) δ ppm 1.4 (s, 9H), 1.6 (d, J=3.4 Hz, 1H), 1.6 (m, 1H), 1.7 (m, 1H), 2.0 (m, 1H), 2.4 (m, 1H), 2.8 (m, 1H), 3.0 (s, 1 H), 3.7 (s, 3H), 3.9 (d, J=13.2 Hz, 1H), 4.1 (s, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07485636B2
Quelldatensatzuspto-grants-2009_02
ORD IDord-370f795a58284cb2b915c4aff436f940
Quellennotizuspto-grants-2009_02