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HRID 8756作成日:2026年10月25日

Propanal → tert-Butyl 4-(3-hydroxy-1-oxopent-1-yl)-4-methoxypiperidine-1-carboxylate

https://huagongshe.com/reaction/8756

反応式

関与物質

役割名称HCID仕込み量
反応物PropanalHCID 527—
反応物Ammonium ChlorideHCID 25517—
反応物Tert-butyl 4-acetyl-4-methoxypiperidine-1-carboxylateHCID 21983927—
反応物Lithium diisopropylamineHCID 45051747—
溶媒TetrahydrofuranHCID 8028—
生成物tert-Butyl 4-(3-hydroxy-1-oxopent-1-yl)-4-methoxypiperidine-1-carboxylateHCID 2198400455.9%

反応手順

To a solution of tert-butyl 4-acetyl-4-methoxypiperidine-1-carboxylate (0.589 g, 2.29 mmol) from Step A in tetrahydrofuran (20 mL) at −78° C. was added lithium diisopropylamine (0.650 mL, 0.974 mmol) followed by propionaldehyde (0.266 g, 0.330 mL, 4.58 mmol). After 5 min, the reaction mixture was poured into saturated ammonium chloride, and extracted three times with diethyl ether. The organic layers were combined, washed with saturated sodium chloride solution, dried over sodium sulfite, filtered, and concentrated. The residue was purified by flash chromatography eluting with 40% ethyl acetate/hexanes to afford the title compound (0.404 g). MS/EI (acetonitrile/water): m/z 216.1 (M+1−BOC) retention time=2.69 min.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07091211B2
出典データセットuspto-grants-2006_08
ORD IDord-b89820f3efd14138aa3a6cb136df92cc
出典メモuspto-grants-2006_08