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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 504399생성일: 2026년 10월 25일

Dimethylformamide → methyl 3-[1-(phenoxyacetyl)-2,3-dihydro-1H-pyrrol-3-yl]benzoate

https://huagongshe.com/reaction/504399

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Ethyl AcetateHCID 8857—
반응물Methyl 3-bromobenzoateHCID 12070—
반응물Potassium AcetateHCID 517044—
반응물Benzyl 3-pyrroline-1-carboxylateHCID 643471—
촉매Tetrabutylammonium BromideHCID 74236—
촉매palladium(II) acetateHCID 167845—
용매WaterHCID 962—
생성물methyl 3-[1-(phenoxyacetyl)-2,3-dihydro-1H-pyrrol-3-yl]benzoateHCID 66662462—

반응 단계

A solution of benzyl 2,5-dihydro-1H-pyrrole-1-carboxylate (0.626 mL, 0.00349 mol), methyl 3-bromo-benzoate (300 mg, 0.001 mol), palladium(II) diacetate (14 mg, 0.000063 mol), potassium acetate (356 mg, 0.00363 mol), and tetra-N-butylammonium bromide (4.50×10−2 mg, 0.00140 mol) in N,N-dimethylformamide (5 mL, 0.06 mol) was stirred under nitrogen at 40° C. for 4 days. The reaction mixture was diluted with AcOEt and water. The organic layer was separated and the aqueous layer was extracted with AcOEt. The combined organic layer was washed with brine, dried with MgSO4, and concentrated to afford the crude product. The crude product was purified by flash chromatography, eluting with 30% AcOEt in hexanes.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07776874B2
출처 데이터셋uspto-grants-2010_08
ORD IDord-508907cfc2de43d58ce1741d2c556de4
출처 메모uspto-grants-2010_08