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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1470970생성일: 2026년 10월 27일

4-Chloroaniline → 1-(4-Chlorophenyl)-2,5-bis(4-nitrophenyl)pyrrolidine

https://huagongshe.com/reaction/1470970

반응식

참여 물질

역할이름HCID투입량
반응물4-ChloroanilineHCID 7812—
반응물TriethylamineHCID 8471—
반응물Methanesulfonyl chlorideHCID 31297—
반응물(1R,4R)-1,4-bis(4-nitrophenyl)butane-1,4-diolHCID 59616924—
용매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물1-(4-Chlorophenyl)-2,5-bis(4-nitrophenyl)pyrrolidineHCID 8664910635.3%

반응 단계

The product of Example 1B (0.50 g, 1.51 mmol) was suspended in CH2Cl2 (15 mL). Triethylamine (0.626 mL, 4.51 mmol) was added at 0° C., the resulting mixture was stirred for 30 min, and methanesulfonyl chloride (0.293 mL, 3.76 mmol) was added. The mixture was stirred at rt for 1 hr and then concentrated in vacuo to give a light yellow solid. The solid was dissolved in DMF (6 mL), 4-chloroaniline (1.92 g, 15.05 mmol) was added, and the resulting mixture was stirred at 50° C. overnight. The mixture was partitioned between EtOAc and 1N aq HCl, and the organic layer was dried over Na2SO4, filtered and concentrated in vacuo. The crude product was purified by column chromatography on silica gel using a solvent gradient of 0-12% EtOAc in hexane to give the title compound (0.226 g, 35%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09006387B2
출처 데이터셋uspto-grants-2015_04
ORD IDord-98a74bb76e304355a55037d989a89499
출처 메모uspto-grants-2015_04