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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1393354생성일: 2026년 10월 26일

2,6-Lutidine → 5-Chloro-2-trifluoromethanesulfonyloxy-3-nitrobenzoic acid

https://huagongshe.com/reaction/1393354

반응식

참여 물질

역할이름HCID투입량
반응물2,6-LutidineHCID 7937—
반응물Trifluoromethanesulfonic anhydrideHCID 67749—
반응물5-Chloro-2-hydroxy-3-nitrobenzoic acidHCID 412078—
용매DichloromethaneHCID 6344—
생성물5-Chloro-2-trifluoromethanesulfonyloxy-3-nitrobenzoic acidHCID 2303392595.2%

반응 단계

2,6-Lutidine (1.83 ml, 15.7 mmol) and trifluoro-methanesulfonic anhydride (3.67 g, 13 mmol) were added dropwise in turn to a solution of methyl ester of 5-chloro-3-nitrosalicylic acid (2.32 g, 10.0 mmol) in methylene chloride (25 ml) with stirring under ice cooling and the mixture was stirred under ice cooling for 0.5 hrs. Methylene chloride (20 ml) and ice water (30 ml) were added to the reaction mixture and the aqueous layer was separated and extracted with methylene chloride. The organic layers were combined, washed with water and dried. The solvent was distilled off under reduced pressure and the residue was purified by column chromatography on silica gel (n-hexane/ethyl acetate=10) to give methyl ester of 5-chloro-2-trifluoromethanesulfonyloxy-3-nitrobenzoic acid (3.33 g, 91%) as a pale yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07345068B2
출처 데이터셋uspto-grants-2008_03
ORD IDord-6c43c697bb934391954883510eedae39
출처 메모uspto-grants-2008_03