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HRID 574619作成日:2026年10月27日

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

https://huagongshe.com/reaction/574619

反応式

関与物質

役割名称HCID仕込み量
反応物AcetaldehydeHCID 177—
反応物Sulfuric acid magnesium salt (1:1)HCID 24083—
反応物4-(Aminomethyl)-1-methylpiperidin-4-olHCID 6484262—
溶媒DichloromethaneHCID 6344—
生成物2,8-Dimethyl-1-oxa-3,8-diazaspiro[4.5]decaneHCID 1975533485.9%

反応条件

温度0 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09034891B2
出典データセットuspto-grants-2015_05
ORD IDord-a667713d7ea740cc8466bb9ded0c2186
出典メモuspto-grants-2015_05