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HRID 225493作成日:2026年10月25日

Hydrochloric Acid → 2-Amino-4-nitrobenzyl alcohol

https://huagongshe.com/reaction/225493

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WaterHCID 962—
反応物4-Nitroanthranilic acidHCID 12076—
反応物Borane;tetrahydrofuranHCID 2723981—
溶媒TetrahydrofuranHCID 8028—
生成物2-Amino-4-nitrobenzyl alcoholHCID 54198—

反応条件

温度65 °C

反応手順

A stirred solution of 2-amino-4-nitrobenzoic acid (Aldrich; 18.2 g, 100 mmol) in dry THF (500 mL) at 20° C., is treated with a solution of borane-THF complex (BH3-THF; Fluka; 100 mL of 1.0 M), dropwise over 45 min to regulate the gas evolution. The mixture is then heated at 65° C. for 2 h. The stirred mixture is then cooled to 0° C., treated with water (20 mL) and warmed to RT. Upon the cessation of gas evolution, hydrochloric acid (20 mL of 12 M) is added and the mixture is then heated at 65° C. for 30 min. The cooled mixture is then concentrated to a volume of circa 150 mL by rotary evaporation under reduced pressure to give a suspension. The suspension is filtered and the precipitate is redissolved in ethyl acetate (500 mL) and washed with saturated aqueous sodium hydrogen carbonate (2×150 mL). The solution is dried (Na2SO4), filtered and the solvent is evaporated off under reduced pressure to yield the crude product which is purified by recrystallisation from ethyl acetate-hexane to give the title compound as a yellow crystalline solid, m.p. 126-128° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07557105B2
出典データセットuspto-grants-2009_07
ORD IDord-8e776da9a4a84ebb940fbc83c1eda31b
出典メモuspto-grants-2009_07