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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1187317Generated: October 27, 2026

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

https://huagongshe.com/reaction/1187317

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetaldehydeHCID 177—
ReactantSulfuric acid magnesium salt (1:1)HCID 24083—
Reactant4-(Aminomethyl)-1-methylpiperidin-4-olHCID 6484262—
SolventDichloromethaneHCID 6344—
Product2,8-Dimethyl-1-oxa-3,8-diazaspiro[4.5]decaneHCID 1975533485.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

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, 11-1, 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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673931B2
Source datasetuspto-grants-2014_03
ORD IDord-b3e07410df6d464fb749c7447ffb0b8f
Source noteuspto-grants-2014_03