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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 618471생성일: 2026년 10월 25일

Nitric Acid → 2-Nitro-5-(2-chloro-alpha,alpha,alpha-trifluoro-4-tolyloxy) benzoic acid

https://huagongshe.com/reaction/618471

반응식

참여 물질

역할이름HCID투입량
반응물Nitric AcidHCID 944—
반응물Sulfuric AcidHCID 1118—
반응물Acetic AnhydrideHCID 7918—
반응물3-(2-Chloro-alpha,alpha,alpha-trifluoro-4-tolyloxy)-benzoic acidHCID 19828811—
용매Butyl AcetateHCID 31272—
생성물2-Nitro-5-(2-chloro-alpha,alpha,alpha-trifluoro-4-tolyloxy) benzoic acidHCID 8674736785%

반응 조건

온도0 °C

반응 단계

Acetic anhydride (37.7 g) was added to 3-(2-chloro-α,α,α-trifluoro-4-tolyloxy)-benzoic acid (86% strength, 45 g) in n-butyl acetate (85.8 g) at 35° C. Sulphuric acid (98%, 12.2 g) was added slowly and the mixture cooled to 0° C. Nitric acid (90%, 10.4 g) was then added slowly over about 3 hours such that the temperature was maintained at -5 to 0° C. On completion of the nitric acid addition the reaction was quenched with water (60 g) at 0° C. The mixture was warmed to 50-60° C. and the aqueous layer removed. The solvent layer was washed with water (2×100 g) at 60° C. and the aqueous layer removed. The solvent and acetic acid were removed by distillation to give 2-nitro-5-(2-chloro-α,α,α-trifluoro-4-tolyloxy) benzoic acid (85%), 2'-nitro isomer (7.5 to 8.5 pph), total dinitro's (~0.5 pph).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05952531
출처 데이터셋uspto-grants-1999_09
ORD IDord-08f7744ce4ec4e63976db311a0570b43
출처 메모uspto-grants-1999_09