돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 127003생성일: 2026년 10월 25일

Hydrochloric Acid → Ethyl 3-hydroxy-4-nitrobenzoate

https://huagongshe.com/reaction/127003

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물EthanolHCID 702—
반응물3-Hydroxy-4-nitrobenzoic acidHCID 69265—
생성물Ethyl 3-hydroxy-4-nitrobenzoateHCID 127845641,492.2%

반응 단계

3-Hydroxy-4-nitrobenzoic acid (20.0 g, 109 mmol) in ethanol (250 mg) was refluxed for 6 hr in the presence of dry hydrogen chloride (5 g). The solvent was evaporated and the residue was dissolved in methylene chloride. The solution was washed with sodium bicarbonate until the unreacted material was removed as a precipitate. The organic fraction was finally washed with brine, dried over magnesium sulfate to give a brown solid of 3- hydroxy-4-nitrobenzoic acid ethyl ester (17.1 g): mp 80°-81° C. (crystallized from diethyl ether-hexane); Anal. Calcd for C9H9NO5 : C, 51.19% H, 4.30% N, 6.63% and Found: C, 51.23% H, 4.30% N, 6.79%; ir(CHCl3) 3,260, 1,720, 1,535 and 1,320 cm-1 ; and nmr(CDCl3)δ 1.35 (3H, t), 4.3 (2H, q), 7.7 (3H, m) and 10.4 (1H, s).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04254118
출처 데이터셋uspto-grants-1981_03
ORD IDord-7c14fff95d394707845974cae316b863
출처 메모uspto-grants-1981_03