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HRID 1814858作成日:2026年10月25日

Acetic Acid → 1-Carbethoxy-4-dimethylamino-3-methylpiperidine

https://huagongshe.com/reaction/1814858

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物FormaldehydeHCID 712—
反応物Sodium cyanoborohydrideHCID 5003444—
反応物Ethyl 4-amino-3-methylpiperidine-1-carboxylateHCID 22278886—
溶媒MethanolHCID 887—
生成物1-Carbethoxy-4-dimethylamino-3-methylpiperidineHCID 22278865—

反応手順

Paraformaldehyde (5.1 g) was added to the stirred solution of 4-amino-1-carbethoxy-3-methylpiperidine (3.5 g, 18.8 mmol) in methanol (100 ml) at 0° C. and sodium cyanoborohydride (1.7 g, 27.0 mmol) was added to it. Then, acetic acid (1 ml) was added to the resulting mixture and stirring was continued for 96 hr at ambient temperature. The reaction mixture was concentrated to dryness, triturated with water, acidified with conc. HCl (pH 3˜4) and extracted with ethyl acetate to remove impurities. The aqueous layer was basified with 1 M sodium hydroxide solution (pH˜10) and extracted with ethyl acetate. Ethyl acetate extract was dried (Na2SO4) and concentrated to dryness to give 1-carbethoxy-4-dimethylamino-3-methylpiperidine. Yield 3.5 g (88%), C11H22N2O2, m/z 215 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06878713B2
出典データセットuspto-grants-2005_04
ORD IDord-a3e30f50970f4993bafcd57770fde36e
出典メモuspto-grants-2005_04