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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 408620Erstellt: 24. Oktober 2026

Acetic Acid → 1-Benzyl-2-methyl-azetidine-2-carboxylic acid ethyl ester

https://huagongshe.com/de/reaction/408620

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktPotassium bis(trimethylsilyl)amideHCID 3251421—
Edukt2-[Benzyl-(2-chloro-ethyl)-amino]-propionic acid ethyl esterHCID 70557779—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-Benzyl-2-methyl-azetidine-2-carboxylic acid ethyl esterHCID 7055865879,1%

Reaktionsbedingungen

Temperatur-76 °C

Reaktionsschritte

A solution of 2-[benzyl-(2-chloro-ethyl)-amino]-propionic acid ethyl ester (27.4 g, 1 eq.) in 253 mL of dry THF was cooled to −78° C. under argon. KHMDS (15% w/w in toluene, 170.40 g, 1.25 eq.) was slowly added so that temperature was kept below −76° C. The reaction was stirred for 1 h at −76° C., then warmed to 20° C. and stirred for 1 h. Acetic acid (1.74 mL, 0.3 eq.) was added and the reaction was stirred at 20° C. for 10 min. The reaction was quenched with 50 mL of a saturated aqueous solution of NaHCO3 and partially concentrated under reduced pressure. The crude was extracted three times with DCM. The organic layers were dried over MgSO4, filtered and concentrated under reduced pressure. The crude was purified by chromatography on silica gel (elution with heptane/EtOAc 100/0 to 90/10) to afford 1-benzyl-2-methyl-azetidine-2-carboxylic acid ethyl ester (18.75 g, yield=79%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08759334B2
Quelldatensatzuspto-grants-2014_06
ORD IDord-65c762b0dd89495094b35cd4931ca45d
Quellennotizuspto-grants-2014_06