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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 427342생성일: 2026년 10월 24일

Triethylamine → Diisopropylether ethyl acetate

https://huagongshe.com/ko/reaction/427342

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Thionyl ChlorideHCID 24386—
반응물4-(Morpholine-4-carbonyl)anilineHCID 577815—
반응물5-Methoxy-8-nitro-1,2,3,4-tetrahydronaphthalene-2-carboxylic acidHCID 18622509—
촉매DimethylformamideHCID 6228—
용매WaterHCID 962—
용매TolueneHCID 1140—
용매DichloromethaneHCID 6344—
생성물N-(4-Morpholinocarbonylphenyl)-5-methoxy-8-nitro-1,2,3,4-tetrahydronaphthalene-2-carboxamideHCID 18622500—
생성물Diisopropylether ethyl acetateHCID 22281796315.3%

반응 조건

온도60 °C

반응 단계

A mixture of 5-methoxy-8-nitro-1,2,3,4-tetrahydronaphthalene-2-carboxylic acid (1.0 g, 4 mmol), toluene (20 mL), N,N-dimethylformamide (10 drops) and thionyl chloride (1.5 mL, 20 mmol) was heated at 60° C. for 1 h. The solvents were removed in vacuo and the residue, dissolved in methylene chloride (20 mL), was added to a solution of 4-aminobenzoylmorpholine (820 mg, 4 mmol, described in: Deylin J. P. J. Chem. Soc. Perkin Trans I, 1975, 830-841) and triethylamine (800 mg, 8 mmol) in methylene chloride (30 mL) at 5° C. After stirring at 20° C. for 2 h, water was added and the organic phase was separated, dried and the solvent removed in vacuo. The oily residue was crystallized from diisopropyl ether/ethyl acetate affording 1.2 g (73% yield) of the title compound as crystals: mp 186-189° C.; EIMS (70 eV) m/z (relative intensity) 439 (20, M+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06313118B1
출처 데이터셋uspto-grants-2001_11
ORD IDord-717ba65c41b6443da0555ea0645bbe72
출처 메모uspto-grants-2001_11