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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 80573생성일: 2026년 10월 24일

Pyridine → Tert-butyl 4-chloro-2-nitrobenzoate

https://huagongshe.com/ko/reaction/80573

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물tert-ButanolHCID 6386—
반응물4-Toluenesulfonyl chlorideHCID 7397—
반응물4-Chloro-2-nitrobenzoic acidHCID 80475—
용매TolueneHCID 1140—
생성물Tert-butyl 4-chloro-2-nitrobenzoateHCID 6389683288.7%

반응 단계

To 4-chloro-2-nitrobenzoic acid (262 g) in a pyridine (1.3 liter) solution, p-toluenesulfonyl chloride (272.6 g) was slowly added at room temperature, and the mixture was stirred at that temperature for 15 minutes. To the reaction solution, tert-butyl alcohol (249 ml) was added dropwise, then the mixture was stirred for 5 hours. To the reaction mixture toluene (1 liter) was added, and the mixture was stirred for 1.5 hours, then the precipitate were removed by filtration. The filtrate was concentrated, ethyl acetate (1.3 liter) was added to the residue, the mixture was successively washed with water, saturated aqueous potassium hydrogensulfate solution, aqueous saturated sodium hydrogencarbonate solution, and brine, then the organic layer was dried over anhydrous sodium sulfate, then concentrated. Methanol (470 ml) was added to the residue, and after the precipitation of the crystals was confirmed, water (142 ml) was added. The mixture was stirred under ice cooling for 1.5 hours, then the crystals were collected by filtration. The same recrystallization procedure as the above was performed again to obtain the title compound (297 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846660B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-550bcabf64c24c0a8f75ae8f00e583db
출처 메모uspto-grants-2014_09