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HRID 225494作成日:2026年10月25日

Allyl bromide → 2-[(2-Propenyloxy)-methyl]-5-nitrobenzenamine

https://huagongshe.com/reaction/225494

反応式

関与物質

役割名称HCID仕込み量
反応物Allyl bromideHCID 7841—
反応物2-Amino-4-nitrobenzyl alcoholHCID 54198—
反応物Potassium tert-butoxideHCID 23665647—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物2-[(2-Propenyloxy)-methyl]-5-nitrobenzenamineHCID 68495687—

反応条件

温度0 °C

反応手順

A stirred solution of 2-amino-4-nitrobenzenemethanol (14.3 g, 85 mmol) in dry THF (350 mL) at 0° C. under an argon atmosphere, is treated dropwise over 35 min with a solution of potassium tert-butylate in THF (Fluka; 85 mL of 1.0 M). The mixture is stirred at 0° C. for 15 min and then treated dropwise over 50 min with a solution of allylbromide (7.9 mL, 94 mmol) in dry THF (80 mL) at 0° C. and then stirred at 20° C. for 90 min. The mixture is diluted with ethyl acetate (800 mL). The resulting solution is washed with saturated aqueous ammonium chloride (3×400 mL), dried (MgSO4), filtered and the solvent is evaporated off under reduced pressure to yield the crude product which is purified by column chromatography on silica gel, eluent 50% ethyl acetate in hexane, to give the title compound as a brown oil.

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-3368b4e0080f4501b090a6f926e165fa
出典メモuspto-grants-2009_07