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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 359849생성일: 2026년 10월 24일

4-Hydroxy-3-nitrobenzoic acid → Isopropyl Acetate

https://huagongshe.com/ko/reaction/359849

반응식

참여 물질

역할이름HCID투입량
반응물4-Hydroxy-3-nitrobenzoic acidHCID 12033—
반응물5-(5-Bromopentyl)-3-methylisoxazoleHCID 13544046—
반응물3-bromo-4-hydroxy-N-(2-hydroxyethyl)-5-nitrobenzamideHCID 20064086—
반응물Methanol isopropylacetateHCID 22498805—
반응물2-Bromo-4-(4,5-dihydro-2-oxazolyl)-6-nitrophenolHCID 135621460—
생성물Isopropyl AcetateHCID 7915—
생성물3-Bromo-4-hydroxy-5-nitrobenzoic acidHCID 20064066—

반응 단계

Intermediates: 5-(5-bromopentyl)-3-methylisoxazole and 2-bromo-4-(4,5-dihydro-2-oxazolyl)-6-nitrophenol. The latter, a bright yellow solid, was prepared by cyclization of 3-bromo-4-hydroxy-N-(2-hydroxyethyl)-5-nitrobenzamide, yellow solid, m.p. 163°-164° C. (from methanol-isopropyl acetate). The latter was in turn prepared by bromination of 4-hydroxy-3-nitrobenzoic acid to form 5-bromo-4-hydroxy-3-nitrobenzoic acid, m.p. 233°-234° C. (yellow solid from isopropyl acetate), esterification to the corresponding methyl ester, m.p. 128°-130° C. (yellow solid from carbon tetrachloride) and reaction of the latter with 2-hydroxyethylamine.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05002960
출처 데이터셋uspto-grants-1991_03
ORD IDord-3479337427864f90ac8b4c6a0f3f1f5b
출처 메모uspto-grants-1991_03