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HRID 423543作成日:2026年10月26日

Diethyl Ether → {1-[3-(1-Methylethyl)-1,2,4-oxadiazol-5-yl]-4-piperidinyl}methanol

https://huagongshe.com/reaction/423543

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl EtherHCID 3283—
反応物4-(Hydroxymethyl)piperidine-1-carbonitrileHCID 51358289—
反応物HCID 178449908HCID 178449908—
触媒ZincchlorideHCID 3007855—
溶媒Ethyl AcetateHCID 8857—
生成物{1-[3-(1-Methylethyl)-1,2,4-oxadiazol-5-yl]-4-piperidinyl}methanolHCID 57930076438%

反応手順

A solution of 1N ZnCl2 in Et2O (182 mL, 182 mmol) was added to a solution of 4-(hydroxymethyl)-1-piperidinecarbonitrile (21.3 g, 152 mmol) and N-hydroxy-2-methylpropanimidamide (18.6 g, 182 mmol) in EtOAc (50 mL) at ambient temperature. The reaction mixture was left at ambient temperature for 30 min, decanted, and was treated with concentrated HCl (45 mL) and ethanol 20 mL). The mixture was heated at reflux for 2 h. The mixture was evaporated to dryness, and the resulting residue was charged with water and the pH was adjusted to basic with K2CO3. The mixture was extracted with EtOAc and the material obtained was combined with 9 other batches prepared similarly and purified by silica gel chromatography to give 150 g of {1-[3-(1-methylethyl)-1,2,4-oxadiazol-5-yl]-4-piperidinyl}methanol.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08101634B2
出典データセットuspto-grants-2012_01
ORD IDord-132c494bbfdd4826bd3d9099cd03ce51
出典メモuspto-grants-2012_01