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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 642147생성일: 2026년 10월 24일

4-Methylmorpholine → Methyl 4-{[3-(1,3-benzodioxol-5-yl)propanoyl]amino}benzoate

https://huagongshe.com/ko/reaction/642147

반응식

참여 물질

역할이름HCID투입량
반응물4-MethylmorpholineHCID 7972—
반응물Methyl 4-aminobenzoateHCID 12082—
반응물Isobutyl chloroformateHCID 62365—
반응물3-(Benzodioxol-5-yl)propionic acidHCID 64810—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
생성물Methyl 4-{[3-(1,3-benzodioxol-5-yl)propanoyl]amino}benzoateHCID 994524462%

반응 단계

To a solution of 3-(3,4-methylenedioxyphenyl)-propionic acid (501 mg, 2.58 mmol) in anhydrous THF (10 mL) were added N-methylmorpholine (0.28 mL, 2.58 mmol) and isobutylchloroformate (0.33 mL, 2.58 mmol) at 0° C. After 30 min, at 0° C., a solution of methyl 4-aminobenzoate (390 mg, 2.58 mmol) in anhydrous THF (2 mL) was added to the reaction mixture. After 30 min the temperature was allowed to warm up to rt and stir for 24 hrs. After extraction with EtOAc (100 mL), washing with HCl (0.1 N, 50 mL) and a saturated aqueous solution of NaHCO3 (50 mL), the organic layer was dried over sodium sulfate and evaporated under vacuo to give a solid. The residue was taken up in Et2O, filtrated and washed with Et2O gave the title compound as a white solid (62%) in 99.4% purity by HPLC (MaxPlot detection between 230 and 400 nm).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07696231B2
출처 데이터셋uspto-grants-2010_04
ORD IDord-022d783b1f5d4d81be1e8acae2189d65
출처 메모uspto-grants-2010_04