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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1962874Erstellt: 25. Oktober 2026

Ethanol → 3-Methyl-3-prop-2-ynyloxymethyl-1-oxa-4-aza-spiro[4.5]decane

https://huagongshe.com/reaction/1962874

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolHCID 702—
EduktPropargyl bromideHCID 7842—
EduktSodium hydrideHCID 24758—
Edukt(3-Methyl-1-oxa-4-azaspiro[4.5]decan-3-yl)methanolHCID 278563—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3-Methyl-3-prop-2-ynyloxymethyl-1-oxa-4-aza-spiro[4.5]decaneHCID 59565408—

Reaktionsschritte

Sodium hydride (55% in dispersion in oil) (0.636 g) was added portion wise to a solution of (3-methyl-1-oxa-4-aza-spiro[4.5]dec-3-yl)-methanol (2.0 g) in dry THF (30 ml) at 0° C. The reaction mixture was stirred at room temperature for 1 h. Propargyl bromide (0.972 ml) was added dropwise at 0° C. and the resulting mixture was stirred at room temperature for 2.5 h. The reaction mixture was treated with ethanol (4 ml) and diluted with diethyl ether and the mixture was filtered. The filtrate was concentrated in vacuo to providing a crude residue which was purified by column chromatography (hexane/ethyl acetate 1:1) to give 2.33 g of 3-methyl-3-prop-2-ynyloxymethyl-1-oxa-4-aza-spiro[4.5]decane as an orange liquid. 1H NMR (CDCl3) δ ppm: 4.18 (2H, d); 3.82 (1H, d); 3.53 (1H, d); 3.43 (1H, d); 3.38 (1H, d); 2.42 (1H, t); 1.7-1.2 (10H, m); 1.25 (1H, s).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08415272B2
Quelldatensatzuspto-grants-2013_04
ORD IDord-9ac805a7f0304a75bebec0420572c058
Quellennotizuspto-grants-2013_04