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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 398086생성일: 2026년 10월 23일

2-Chloro-1-fluoro-4-nitrobenzene → 2-chloro-1-(methylsulfanyl)-4-nitrobenzene

https://huagongshe.com/ko/reaction/398086

반응식

참여 물질

역할이름HCID투입량
반응물2-Chloro-1-fluoro-4-nitrobenzeneHCID 67688—
반응물Sodium methanethiolateHCID 4378561—
촉매SantonoxHCID 7308—
용매DimethylformamideHCID 6228—
생성물2-chloro-1-(methylsulfanyl)-4-nitrobenzeneHCID 1056009452.3%

반응 단계

To a solution of 4-fluoro-3-chloronitrobenzene (27 g, 156 mmol) in DMF (150 mL) at room temperature was added 5-tert-butyl-4-hydroxy-2-methylphenyl sulfide (100 mg) followed by sodium thiomethoxide (NaSMe) (10 g, 143 mmol) and the reaction was stirred for 6 h. The DMF was removed in vacuo and the residue was partitioned between ether (1 L) and water (1 L). The ether layer was washed with water (1 L) and brine (1 L), dried (MgSO4) and the solvent was removed under reduced pressure. The residue was purified by column chromatography (SiO2; DCM: pentane 1:5 increasing polarity to 3:7) to give the title compound (15.22 g, 49%) as a yellow solid; δH (400 MHz, CDCl3) 2.53 (3H, s), 7.20 (1H, d), 8.09 (1H, dd), 8.20 (1H, d).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06610747B2
출처 데이터셋uspto-grants-2003_08
ORD IDord-76eb74a912a34d528fe9645b42d50541
출처 메모uspto-grants-2003_08