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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1892046Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1892046

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 R.T. for 50′. Propargyl bromide (0.972 ml) was added dropwise at 0° C. and the resulting mixture was stirred at R.T. for 2 h 30. Additional sodium hydride (55% in dispersion in oil) (0.047 g) and propargyl bromide (0.081 ml) were added at 0° C. followed by the heating of the reaction mixture at 40-45° C. for 1 hr allowed to reach reaction completion. The reaction mixture was treated with abs. Ethanol (4 ml) and diluted with diethyl ether. The resulting insoluble residue was filtered off and the filtrate was concentrated in vacuo to give 2.89 g of crude residue which was purified by column chromatography (hexane/ethyl acetate 1:1) to yield 2.33 g of 3-Methyl-3prop-2-ynyloxymethyl-1-oxa-4-aza-spiro[4.5]decane as an orange liquid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08507509B2
Quelldatensatzuspto-grants-2013_08
ORD IDord-0e5c6747128c4bb480cc197d76148dbe
Quellennotizuspto-grants-2013_08