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HRID 1199182Erstellt: 25. Oktober 2026

Benzene → trans-1-Methyl-3-diethylamino-4-phenyl-2-azetidinone

https://huagongshe.com/reaction/1199182

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzeneHCID 241—
EduktAmmonium ChlorideHCID 25517—
EduktGlycine, N,N-diethyl-, ethyl esterHCID 75843—
EduktEthenamine, 2-phenyl-HCID 155076—
LösungsmittelDiethyl EtherHCID 3283—
Produkttrans-1-Methyl-3-diethylamino-4-phenyl-2-azetidinoneHCID 1426216095%

Reaktionsschritte

2.95 g (10 mmoles) of the ethylzinc enolate lithium chloride complex of N,N-diethylglycine ethyl ester (the product obtained from example I) was dissolved in 20 ml benzene at room temperature. To this clear colourless solution was added 1.19 g (10 mmoles) of N-(benzylidene)methylamine. The resulting solution was refluxed for 30 min. During this period some precipitate formed. The reaction mixture was cooled to room temperature and diluted with 25 ml diethyl ether. To this mixture, 10 ml of a saturated aqueous ammonium-chloride solution was added. The aqueous layer was separated and the organic layer was twice washed with 10 ml of an aqueous ammonium chloride solution and twice with 10 ml portions of water, dried over sodium sulfate and concentrated in vacuo yielding 2.2 g (95%) of the 2-azetidinone product as a white solid with the properties: m.p. 70°-71° C. 1H NMR (60 MHz, CDCl3): δ7.30 (m, 5H, arom.), 4.60 (d, J=1.6 Hz, 1H, NCHCHPh), 4.10 (d, J=1.6 Hz, 1H, NCHCHPh), 2.90 (s, 3H, NCH3), 2.90 (q, 4H, NCH2CH3), 1.15 (t, 6H, NCH2CH3).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04898955
Quelldatensatzuspto-grants-1990_02
ORD IDord-230bca7aec914bceacdf0b22d937f7a7
Quellennotizuspto-grants-1990_02