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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 30313생성일: 2026년 10월 23일

Benzylethanolamine → 4-Benzylmorpholine-2-carboxylic acid hydrochloride

https://huagongshe.com/ko/reaction/30313

반응식

참여 물질

역할이름HCID투입량
반응물BenzylethanolamineHCID 4348—
반응물TetrahydrofuranHCID 8028—
반응물2-ChloroacrylonitrileHCID 70198—
반응물Potassium tert-butoxideHCID 23665647—
용매TolueneHCID 1140—
생성물4-Benzylmorpholine-2-carboxylic acid hydrochlorideHCID 277635261%

반응 단계

A 500 mL reactor under N2 is successively loaded with toluene (36.72 mL) and 2-chloroacrylonitrile (10.7 g, 122.23 mmol) at room temperature. Then, N-benzyl ethanolamine (18.36 g, 121.14 mmol) is added over 5 min and the reaction mixture is post-agitated at room temperature for 16 h. Then, the mixture is diluted with toluene (110.16 mL), cooled to −5° C. and 2M potassium tert-butoxide solution in THF (121.14 mmol) is slowly added over 30 min, maintaining the temperature at −5° C. to 0° C. The mixture is post-agitated at about −5° C. to 0° C. for 1 h, then quenched by adding water (45.9 mL). The aqueous layer is separated and the toluene layer is washed with water (45.9 mL) and then the mixture is allowed to warm to room temperature. The organic layer is then concentrated under reduced pressure at 40° C. Then, the mixture is diluted with toluene (100 mL) and extracted with 6N HClaq (162 mL). This aqueous layer is heated up to the reflux for 1 h 30, then the mixture is allowed to stir at room temperature overnight. After crystallization of 91, the solid is filtered, rinsed with 6N HClaq (40 mL) and dried under reduce pressure at 40° C. (19 g, yield=61%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07423037B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-54fa4ad3018b43109b1c48ab5b1d7e67
출처 메모uspto-grants-2008_09