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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 30314생성일: 2026년 10월 25일

Dimethylformamide → N-benzyl-2-(morpholin-4-carbonyl)-morpholine hydrochloride

https://huagongshe.com/reaction/30314

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물MorpholineHCID 8083—
반응물Oxalyl chlorideHCID 65578—
반응물4-Benzylmorpholine-2-carboxylic acid hydrochlorideHCID 2776352—
용매1,1-DichloroethaneHCID 6365—
생성물N-benzyl-2-(morpholin-4-carbonyl)-morpholine hydrochlorideHCID 68436268—

반응 조건

온도62.5 °C

반응 단계

A 250 mL reactor under N2 is successively loaded with 91 (5 g, 19.41 mmol), dichloroethane (50 mL), DMF (0.014 mL, 1% mol) and oxalyl chloride (1.86 mL, 21.35 mmol). The mixture is heated up to 60-65° C. for 2 h, before being cooled to 0° C. Then, morpholine (6.93 g, 79.60 mmol) in dichloroethane (20 mL) is added over 15 min keeping the temperature below 10° C. The heterogeneous solution is post-agitated for 1 h 30 min at room temperature and quenched with water (30 mL). The biphasic mixture is filtered on a Hyflo Super Cel® (10 g), then after separation, the organic layer is concentrated under reduce pressure. The mixture is taken up with isopropanol (80 mL) and 12N HClaq (1.61 mL, 19.41 mmol), stirred for 10 min and concentrated under reduce pressure. The mixture is taken up with isopropanol (13 mL), heated to reflux until a homogeneous solution is formed, then it is cooled to room temperature. The precipitate is filtered, rinsed with isopropanol (10 mL) and dried under vacuum at 40° C. overnight to obtain 92 as an off-white powder with 79% overall yield.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07423037B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-427226a221e043c0b74882f62f2c6aba
출처 메모uspto-grants-2008_09