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HRID 720796作成日:2026年10月23日

Hydrochloric Acid → 5-bromo-1H-indazole

https://huagongshe.com/ja/reaction/720796

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4-Bromo-2-methylanilineHCID 11423—
反応物18-Crown-6HCID 28557—
反応物Potassium AcetateHCID 517044—
反応物Ammonium fluoroborateHCID 9964072—
反応物Sodium NitriteHCID 23668193—
溶媒Acetic AcidHCID 176—
生成物5-bromo-1H-indazoleHCID 761929152.3%

反応条件

温度0 °C

反応手順

Ammonium tetrafluoroborate (20.97 g, 200 mmol) was dissolved in aqueous acetic acid (500 mL AcOH/250 mL water) and cooled to 0° C. 2-Methyl-4-bromoaniline (18.61 g, 100 mmol) and 42 mL of aqueous concentrated HCl (36% w/w, 12N, 500 mmol) were sequentially added. The mixture was stirred for 20 minutes at 0° C. and NaNO2 (7.59 g, 110 mmol) was added. The reaction was stirred for 1 hour at 0° C. and warmed to room temperature. After 16 hours at room temperature, the mixture was concentrated under reduced pressure and the residue was azeotroped with toluene and dried under high vacuum. The solid was suspended in 500 mL of CHCl3 and KOAc (12.76 g, 130 mmol) and 18-crown-6 (7.93 g, 30 mmol) were added. The reaction was stirred for 1.5 hours at room temperature. The mixture was washed with water, dried over anhydrous MgSO4, filtered through Celite and concentrated under reduced pressure to provide 30 g of 5-bromo-1H-indazole (compound 2f) as a tan solid. The crude material was used without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07135575B2
出典データセットuspto-grants-2006_11
ORD IDord-924b49e471344ffe8b7901bf7b61955d
出典メモuspto-grants-2006_11