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HRID 20216생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/20216

반응식

참여 물질

역할이름HCID투입량
반응물EthanolamineHCID 700—
반응물Sodium HydroxideHCID 14798—
반응물Benzyl 4-oxopiperidine-1-carboxylateHCID 643496—
반응물Sodium triacetoxyborohydrideHCID 5049666—
용매1,2-DichloroethaneHCID 11—
용매Acetic AcidHCID 176—
용매MethanolHCID 887—
생성물Benzyl 4-[(2hydroxyethyl)amino]piperidin-1-carboxylateHCID 22137568107.7%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745623B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-75db2ba6c6b64dc88b6623abe37c1296
출처 메모uspto-grants-2010_06