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HRID 653398Erstellt: 24. Oktober 2026

Methyl Acrylate → 4,5-Dihydro-5-(methoxycarbonyl)-3-isoxazolepropanoic acid methyl ester

https://huagongshe.com/de/reaction/653398

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl AcrylateHCID 7294—
EduktPhenyl isocyanateHCID 7672—
EduktTriethylamineHCID 8471—
EduktMethyl 4-nitrobutyrateHCID 25604—
LösungsmittelTolueneHCID 1140—
Produkt4,5-Dihydro-5-(methoxycarbonyl)-3-isoxazolepropanoic acid methyl esterHCID 13911553—

Reaktionsschritte

A solution of 23.8 g of 4-nitrobutyric acid methyl ester (made in accordance with Bruson, U.S. Pat. No. 2,342,119) 39.6 g of methyl acrylate, 0.2 g triethyl amine in 200 ml of toluene is stirred and treated dropwise with 23.8 g of phenyl isocyanate. The mixture is stirred for 72 hours at room temperature and heated at 90° C. for two hours. The mixture is cooled, filtered to remove the diphyl urea, and concentrated under reduced pressure. The resulting oil is chromatographed on SiO2 (elution with hexane:ethyl-acetate; 75:25) to yield 4,5-dihydro-5-(methoxycarbonyl)-3-isoxazolepropanoic acid methyl ester as a colorless oil. NMR (CDCl3) and 4.93 (t, J=9 Hz, 1H), 3.72 (s, 3H), 3.63 (s, 3H), 3.20 (d, J-9 Hz, 2H9, 2.61 (s, 4H). IR (KBr) 2956, 2851, 1739, 1632, 1439, 1367, 1340, 1215. IR (cm-1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04677098
Quelldatensatzuspto-grants-1987_06
ORD IDord-39b3ead62885473aac7b69884bfc2550
Quellennotizuspto-grants-1987_06