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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 18606생성일: 2026년 10월 24일

Triethylamine → (3-Fluoro-4-nitro-phenyl)-pyrrolidin-1-yl-methanone

https://huagongshe.com/ko/reaction/18606

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Thionyl ChlorideHCID 24386—
반응물PyrrolidineHCID 31268—
반응물3-Fluoro-4-nitrobenzoic acidHCID 230653—
촉매DimethylformamideHCID 6228—
용매BenzeneHCID 241—
용매DichloromethaneHCID 6344—
생성물(3-Fluoro-4-nitro-phenyl)-pyrrolidin-1-yl-methanoneHCID 55103417—

반응 조건

온도70 °C

반응 단계

1.00 g (5.40 mmol) 3-Fluoro-4-nitro-benzoic acid were suspended in 55 mL benzene. 1 mL Thionyl chloride and 7 drops DMF were added. The resulting mixture was stirred of 5 h at 70° C. and then concentrated under reduced pressure. The residue was dissolved in 40 mL CH2Cl2. Subsequently 0.75 mL (5.40 mmol) triethylamine and 0.45 mL (5.40 mmol) pyrrolidine were added and the resulting solution was stirred for 1 h at room temperature. The mixture was diluted with CH2Cl2 and washed subsequently with a 0.1 N HCl-solution, with a saturated NaHCO3-solution and with brine. The organic layer was dried over anhydrous MgSO4 and concentrated under vacuo to give crude (3-Fluoro-4-nitro-phenyl)-pyrrolidin-1-yl-methanone as an orange solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07741341B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-5f9779b5c3244eb2a6fd38a7490201d2
출처 메모uspto-grants-2010_06