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HRID 467808생성일: 2026년 10월 26일

Methyl 2-ethoxy-4-nitrobenzoate → 2-Ethoxy-4-aminobenzoic acid

https://huagongshe.com/reaction/467808

반응식

참여 물질

역할이름HCID투입량
반응물Methyl 2-ethoxy-4-nitrobenzoateHCID 9964566—
촉매NickelHCID 935—
용매MethanolHCID 887—
생성물2-Ethoxy-4-aminobenzoic acidHCID 10176385108%

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-894e0d98b9024962912db9c3abb6445b
출처 메모uspto-grants-2014_01