戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 44641作成日:2026年10月23日

Triphenylphosphine → N-[3-(1-Methyl-piperidin-4-yloxy)-phenyl]-acetamide

https://huagongshe.com/ja/reaction/44641

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物3-HydroxyacetanilideHCID 12124—
反応物4-Piperidinol, 1-methyl-HCID 66048—
溶媒TetrahydrofuranHCID 8028—
生成物N-[3-(1-Methyl-piperidin-4-yloxy)-phenyl]-acetamideHCID 57444159—

反応手順

A suspension of N-(3-Hydroxy-phenyl)-acetamide (30.2 g) in anhydrous tetrahydrofuran (600 mL) was treated with 4-hydroxy-N-methylpiperidine (30.54 mL) and triphenylphosphine (68.18 g); a solution of diethylazadicarboxylate in anhydrous tetrahydrofuran (THF) (40.94 mL in 60 mL of THF) was added dropwise and the mixture was stirred at room temperature for 2 hours and then heated to 50° C. overnight. Further amounts of triphenylphosphine (28.00 g) and diethylazadicarboxylate (14 mL) were added and the heating was continued for additional 24 hours.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08541429B2
出典データセットuspto-grants-2013_09
ORD IDord-c4473f8be0684334b827e5bd7897e708
出典メモuspto-grants-2013_09