戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 20216作成日:2026年10月25日

Ethanolamine → Benzyl 4-[(2hydroxyethyl)amino]piperidin-1-carboxylate

https://huagongshe.com/reaction/20216

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolamineHCID 700—
反応物Sodium HydroxideHCID 14798—
反応物Benzyl 4-oxopiperidine-1-carboxylateHCID 643496—
反応物Sodium triacetoxyborohydrideHCID 5049666—
溶媒1,2-DichloroethaneHCID 11—
溶媒Acetic AcidHCID 176—
溶媒MethanolHCID 887—
生成物Benzyl 4-[(2hydroxyethyl)amino]piperidin-1-carboxylateHCID 22137568107.7%

反応手順

A solution of benzyl 4-oxopiperidin-1-carboxylate (7.0 g), 2-aminoethanol (2.8 g) and acetic acid (2.7 g) in 1,2-dichloroethane (150 mL)-methanol (10 mL) was stirred at room temperature for 3 hours, sodium triacetoxyborohydride (12.7 g) was added thereto, and the mixture was stirred at room temperature for 15 hours. A 1N sodium hydroxide solution was added to the reaction mixture, pH of the aqueous layer was adjusted to about 12, and then the organic layer was separated. The organic layer was dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure to obtain the title compound (9.0 g, quantitative) as a colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07745623B2
出典データセットuspto-grants-2010_06
ORD IDord-75db2ba6c6b64dc88b6623abe37c1296
出典メモuspto-grants-2010_06