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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 408578Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/408578

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 70558658—

Reaktionsbedingungen

Temperatur-70 °C

Reaktionsschritte

A solution of 2-[benzyl-(2-chloro-ethyl)-amino]-propionic acid ethyl ester (1 eq.) in dry THF was cooled to −78° C. under nitrogen. KHMDS (15% w/w in toluene) (1.25 eq.) was slowly added so that temperature was kept below −65° C. The reaction was stirred for 1 h at −70° C. Then acetic acid (0.3 eq.) was added. The reaction was warmed to 20° C. and stirred for 10 min, then quenched with a saturated aqueous solution of NaHCO3 and partially concentrated under reduced pressure. The crude was extracted twice with DCM. The organic layers were combined, dried over MgSO4, filtered and concentrated under reduced pressure. The crude was purified by chromatography on silica gel (elution with heptane/EtOAc 1/0 then 95/5) to afford 1-benzyl-2-methyl-azetidine-2-carboxylic acid ethyl ester.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08759334B2
Quelldatensatzuspto-grants-2014_06
ORD IDord-f490badee2424203bebb3fd33a4da7a0
Quellennotizuspto-grants-2014_06