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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 323055생성일: 2026년 10월 24일

Triethylamine → N-(2-hydroxy-4-nitrophenyl)-N'-(2,3-methylenedioxyphenyl)urea

https://huagongshe.com/ko/reaction/323055

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참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물P,P-Diphenylphosphinic azideHCID 199401—
반응물1,3-Dioxaindane-4-carboxylic acidHCID 304832—
반응물2-Amino-5-NitrophenolHCID 4984721—
용매TolueneHCID 1140—
생성물N-(2-hydroxy-4-nitrophenyl)-N'-(2,3-methylenedioxyphenyl)ureaHCID 988343242%

반응 조건

온도60 °C

반응 단계

To a solution of the 2,3-methylenedioxyphenylcarboxylic acid in toluene, triethylamine (0.27 mL, 1.95 mmol) and diphenylphosphoryl azide (DPPA) (0.32, mL, 1.5 mmol) were added. The reaction mixture was stirred at 60° C. for 2 hours, then 2-amino-5-nitrophenol (250 mg, 1.5 mmol) was added. The reaction mixture was stirred at 100° C. for 18 hours. After the reaction mixture was cooled to room temperature, it was partitioned between 5% citric acid and ethyl acetate. The organic layer was separated and the aqueous layer was extracted three times with ethyl acetate. The organic extracts were combined, dried over MgSO4, filtered and concentrated under reduced pressure. Chromatography of the resulting solid on silica gel (hexane:ethyl acetate; 5:1) gave product (200 mg, 42%). EI-MS m/z 318 (M+H)+

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06211373B1
출처 데이터셋uspto-grants-2001_04
ORD IDord-ef0995265c31454f9a3e3ffc16bdabb9
출처 메모uspto-grants-2001_04