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HRID 467807作成日:2026年10月26日

Hydrochloric Acid → Methyl 2-ethoxy-4-nitrobenzoate

https://huagongshe.com/reaction/467807

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Ethyl BromideHCID 6332—
反応物Potassium CarbonateHCID 11430—
反応物Thionyl ChlorideHCID 24386—
反応物4-Nitrosalicylic acidHCID 69266—
反応物Salicylic acid, 4-nitro-, methyl esterHCID 139539—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物Methyl 2-ethoxy-4-nitrobenzoateHCID 996456626.2%

反応条件

温度50 °C

反応手順

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)+].

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08623887B2
出典データセットuspto-grants-2014_01
ORD IDord-7ad552fd00d54d15b842f50b5836d461
出典メモuspto-grants-2014_01