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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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Acetaldehyde | HCID 177 | — |
| Edukt | Sulfuric acid magnesium salt (1:1) | HCID 24083 | — |
| Edukt | 4-(Aminomethyl)-1-methylpiperidin-4-ol | HCID 6484262 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 2,8-Dimethyl-1-oxa-3,8-diazaspiro[4.5]decane | HCID 19755334 | 85,9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09034891B2 |
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| Quelldatensatz | uspto-grants-2015_05 |
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| ORD ID | ord-a667713d7ea740cc8466bb9ded0c2186 |
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| Quellennotiz | uspto-grants-2015_05 |
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