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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Nitric Acid | HCID 944 | — |
| 반응물 | m-Chlorophenethylic alcohol | HCID 78856 | — |
| 반응물 | Methyl 3-hydroxy-4-methoxybenzoate | HCID 4056967 | — |
| 반응물 | 3-[2-(3-Chloro-phenyl)-ethoxy]-4-methoxy-benzoic acid methyl ester | HCID 67076296 | — |
| 생성물 | 5-[2-(3-Chloro-phenyl)-ethoxy]-4-methoxy-2-nitro-benzoic acid methyl ester | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09328071B2 |
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| 출처 데이터셋 | uspto-grants-2016_05 |
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| ORD ID | ord-fc3fa8a1cef34d83aa89e4341f66f39d |
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| 출처 메모 | uspto-grants-2016_05 |
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