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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 467807생성일: 2026년 10월 25일

Hydrochloric Acid → Methyl 2-ethoxy-4-nitrobenzoate

https://huagongshe.com/reaction/467807

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Ethyl BromideHCID 6332—
반응물Potassium CarbonateHCID 11430—
반응물Thionyl ChlorideHCID 24386—
반응물4-Nitrosalicylic acidHCID 69266—
반응물Salicylic acid, 4-nitro-, methyl esterHCID 139539—
용매MethanolHCID 887—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물Methyl 2-ethoxy-4-nitrobenzoateHCID 996456626.2%

반응 조건

온도50 °C

반응 단계

4.05 g (21.7 mmol, 1 eq) 2-hydroxy-4-nitro-benzoic acid are dissolved in 40 mL MeOH and 1.8 mL (24.8 mmol, 1.14 eq) thionyl chloride are slowly added dropwise. The mixture is refluxed for 2 h at 50° C. and stirred for another 2 h. After cooling the volatile constituents are eliminated in vacuo and 4.36 g of the crude methyl 2-hydroxy-4-nitro-benzoate are obtained, which are reacted without further purification. 1 g (5.1 mmol, 1 eq) of the methyl ester are dissolved in 25 mL DMF, 2.1 g (15.3 mmol, 3 eq) potassium carbonate are added and then 1.4 mL (18.8 mmol, 3.7 eq) bromoethane are added dropwise. The reaction mixture is stirred for 16 h at RT, then poured into 100 mL water and the pH is adjusted with concentrated aqueous hydrochloric acid to pH 3. It is extracted twice with 100 mL EE, dried on MgSO4 and after the elimination of all the volatile constituents in vacuo 1.28 g of methyl 2-ethoxy-4-nitro-benzoate are obtained. 1.28 g (5.06 mmol, 1 eq) of the nitro compound are dissolved in 50 mL MeOH, a spatula tip of Raney nickel is added and the reaction mixture is stirred in the autoclave under a hydrogen pressure of 4 bar for 16 h. The catalyst is filtered off through Celite® and the filtrate is freed in vacuo of all the volatile constituents. 0.99 g of the aniline are obtained [MS-ESI+: 351 (M+H)+].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08623887B2
출처 데이터셋uspto-grants-2014_01
ORD IDord-7ad552fd00d54d15b842f50b5836d461
출처 메모uspto-grants-2014_01