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HRID 574619Erstellt: 26. Oktober 2026

Acetaldehyde → 2,8-Dimethyl-1-oxa-3,8-diazaspiro[4.5]decane

https://huagongshe.com/reaction/574619

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetaldehydeHCID 177—
EduktSulfuric acid magnesium salt (1:1)HCID 24083—
Edukt4-(Aminomethyl)-1-methylpiperidin-4-olHCID 6484262—
LösungsmittelDichloromethaneHCID 6344—
Produkt2,8-Dimethyl-1-oxa-3,8-diazaspiro[4.5]decaneHCID 1975533485,9%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a solution of 4-aminomethyl-1-methyl-piperidin-4-ol (2.127 g, 14.77 mmol) in dichloromethane (15 ml) was added anhydrous magnesium sulfate (2.9 g). The resulting mixture was cooled to 0° C. and freshly distilled acetaldehyde (835 μl, 14.78 mmol) was added. After 6 h of stirring at room temperature, the mixture was filtered and the solvent was evaporated under reduced pressure to give the title compound (2.16 g) as an almost colorless liquid. 1H NMR (CDCl3, 500 MHz) δ 4.60 (q, J=5.40 Hz, 1H, CHCH3), 3.01 (d, J=12 Hz, 1H, CHHNH), 2.76 (d, J=12 Hz, 1H, CHHNH), 2.55-2.31 (m, 4H, CH2N), 2.28 (s, 3H, NCH3), 1.77-1.58 (m, 4H, CH2CO), 1.36 (d, J=5.40 Hz, 3H, CH3CH) ppm; 13C NMR (CDCl3, 300 MHz) δ 87.57 (CH), 57.19 (CH2), 53.14 (C), 52.96 (CH2), 46.15 (CH3), 37.28 (CH2), 35.73 (CH2), 20.32 (CH3) ppm.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09034891B2
Quelldatensatzuspto-grants-2015_05
ORD IDord-a667713d7ea740cc8466bb9ded0c2186
Quellennotizuspto-grants-2015_05