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HRID 1041645作成日:2026年10月27日

Acetic Acid → 2-Ethylamino-4-fluoro-5-nitro-phenol

https://huagongshe.com/reaction/1041645

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物Sodium BicarbonateHCID 516892—
反応物Sodium borohydrideHCID 4311764—
反応物5-Fluoro-2-methyl-6-nitro-1,3-benzoxazoleHCID 13627700—
溶媒TetrahydrofuranHCID 8028—
生成物2-Ethylamino-4-fluoro-5-nitro-phenolHCID 6726362684.4%

反応手順

5-Fluoro-2-methyl-6-nitro-benzoxazole (2.556 g, 13.03 mmol) was dissolved in Tetrahydrofuran (90 mL) and Acetic acid (4.5 mL, 79 mmol). Sodium borohydride (1.48 g, 39.1 mmol) was added and the reaction was stirred at room temperature for 90 min, then poured into 100 mL satd. sodium bicarbonate. The solution was extracted 3×50 mL DCM and the combined organics were washed with 1:1 brine:satd. sodium bicarbonate (50 mL) and dried over sodium sulfate, then conc. onto 10 g Celite. The crude product was chromatographed (120 g silica gel, ISCO, 0-20-40% EtOAc:Hex) to afford 2-Ethylamino-4-fluoro-5-nitro-phenol as a yellow solid (2.20 g, 84%). 1H-NMR (CDCl3): 7.55 (d, 1H, J=6.8 Hz), 6.26 (d, 1H, J=13.2 Hz), 5.51 (s, 1H), 5.05 (s, 1H), 3.26 (m, 2H), 1.34 (t, 3H, J=6.8 Hz).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08552186B2
出典データセットuspto-grants-2013_10
ORD IDord-8995be8133c2489f9acb637fda7fc1be
出典メモuspto-grants-2013_10