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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 553402생성일: 2026년 10월 24일

Triethylamine → 3-hydroxy-N-(2-nitrobenzyl)-3-phenyl propionic acid amide

https://huagongshe.com/ko/reaction/553402

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물3-Hydroxy-3-phenylpropanoic acidHCID 92959—
반응물4-(4,6-Dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chlorideHCID 2734059—
반응물(2-Nitrophenyl)methanamine hydrochlorideHCID 12235442—
반응물Hydrate;hydrochlorideHCID 21885828—
용매TetrahydrofuranHCID 8028—
생성물3-hydroxy-N-(2-nitrobenzyl)-3-phenyl propionic acid amideHCID 6746189492.1%

반응 단계

2-Nitrobenzyl amine hydrochloride (2.27 g, 12.0 mmol), 3-hydroxy-3-phenyl propionic acid (2.00 g, 12.0 mmol), triethylamine (1.34 g, 13.3 mmol) were added to tetrahydrofuran (50 ml) and the reaction mixture was ice cooled. Under ice cooled condition, 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride (3.33 g, 12.0 mmol) was added thereto and stirred at room temperature for five hours. The reaction mixture was poured into dilute hydrochloric acid water and extracted with ethyl acetate. The organic layer was washed with a saturated brine and then dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The obtained crude crystal was washed with a mixture of hexane-ether (2:1) to obtain 3-hydroxy-N-(2-nitrobenzyl)-3-phenyl propionic acid amide (3.32 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08048825B2
출처 데이터셋uspto-grants-2011_11
ORD IDord-fc313c2da70d4e3490790ff94c8806ae
출처 메모uspto-grants-2011_11