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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 521455생성일: 2026년 10월 26일

Nitric Acid → 5-[2-(3-Chloro-phenyl)-ethoxy]-4-methoxy-2-nitro-benzoic acid methyl ester

https://huagongshe.com/reaction/521455

반응식

참여 물질

역할이름HCID투입량
반응물Nitric AcidHCID 944—
반응물m-Chlorophenethylic alcoholHCID 78856—
반응물Methyl 3-hydroxy-4-methoxybenzoateHCID 4056967—
반응물3-[2-(3-Chloro-phenyl)-ethoxy]-4-methoxy-benzoic acid methyl esterHCID 67076296—
생성물5-[2-(3-Chloro-phenyl)-ethoxy]-4-methoxy-2-nitro-benzoic acid methyl esterHCID 67076791—

반응 단계

Methyl 3-hydroxy-4-methoxybenzoate and 2-(3-chlorophenyl)-ethanol were reacted in analogy to step 1 of example 1. The obtained 3-[2-(3-chloro-phenyl)-ethoxy]-4-methoxy-benzoic acid methyl ester (0.750 g, 2.34 mmol) was added slowly to ice-cooled 100% nitric acid (10 ml). The ice bath was removed and stirring was continued overnight. The mixture was cautiously transferred into a stirred mixture of EA, water and an excess of sodium hydrogencarbonate and extracted with EA. The combined organic extracts were washed with a saturated sodium chloride solution, dried over sodium sulfate, filtered and evaporated to dryness. The solid residue was extracted with diethyl ether, and the ethereal solution was evaporated. The residue was stirred with HEP, and the solid was filtered and dried in vacuo to give 0.680 g of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09328071B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-fc3fa8a1cef34d83aa89e4341f66f39d
출처 메모uspto-grants-2016_05