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HRID 926475作成日:2026年10月26日

Acetic Anhydride → 1-Acetyl-4-benzoylpiperidine

https://huagongshe.com/reaction/926475

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AnhydrideHCID 7918—
反応物TriethylamineHCID 8471—
反応物4-Benzoylpiperidine hydrochlorideHCID 2724437—
溶媒DichloromethaneHCID 6344—
生成物1-Acetyl-4-benzoylpiperidineHCID 2740714—

反応手順

A mixture of phenyl(piperidin-4-yl)methanone hydrochloride (743 mg, 3.29 mmol) in dichloromethane (13.2 mL) and triethylamine (1.10 mL, 7.90 mmol) was treated with Ac2O (0.373 mL, 3.95 mmol) dropwise over 1 minute in an ice bath under argon, and the resulting translucent mixture was immediately removed from the ice bath and stirred at room temperature overnight. The reaction was then extracted with 1 M aqueous HCl (1×8 mL) and 1 M aqueous NaOH (1×8 mL), and the organic layer was dried (Na2SO4), filtered, and concentrated to provide the title compound as a translucent beige oil that crystallized upon standing.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09284308B2
出典データセットuspto-grants-2016_03
ORD IDord-fa50c2a622f64a64a1a7a01dcbcfa1c7
出典メモuspto-grants-2016_03