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HRID 225767作成日:2026年10月26日

Acetic Acid → Ammonia

https://huagongshe.com/reaction/225767

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AcetoneHCID 180—
反応物Piperidin-4-olHCID 79341—
反応物Sodium triacetoxyborohydrideHCID 5049666—
溶媒TetrahydrofuranHCID 8028—
生成物AmmoniaHCID 222—
生成物1-Isopropylpiperidin-4-olHCID 79681—

反応手順

A mixture of 4-hydroxypiperidine (10 g, 0.10 mol), acetone (21.8 mL, 0.30 mol), acetic acid (5.7 mL, 0.10 mol) and tetrahydrofuran (150 mL) was stirred in an ice bath for 15 minutes. Sodium triacetoxyborohydride (31.3 g, 0.15mol) was then added portionwise and the mixture was stirred for a further 10 minutes. The reaction mixture was then warmed and stirred at room temperature for 10 minutes and at 40° C. for 2.5 hours. The solvent was evaporated under reduced pressure and the residue was dissolved in water (50 mL). The aqueous solution was basified to pH9 with 0.88 ammonia and the solution was stirred for 30 minutes. The reaction mixture was then extracted with diethyl ether (2×200 mL) and the combined extracts were dried over sodium sulfate and concentrated in vacuo to give a yellow oil. The oil was purified by column chromatography on silica gel, eluting with dichloromethane:methanol:0.88 ammonia, 96:4:1 to 90:10:1, to afford the title product as a yellow oil in quantitative yield, 14.6 g.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07557121B2
出典データセットuspto-grants-2009_07
ORD IDord-b546bb7d2476469faddf9cb39b706090
出典メモuspto-grants-2009_07