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HRID 720797생성일: 2026년 10월 24일

Hydrochloric Acid → 5-bromo-1H-indazole

https://huagongshe.com/ko/reaction/720797

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물4-Bromo-2-methylanilineHCID 11423—
반응물18-Crown-6HCID 28557—
반응물Potassium AcetateHCID 517044—
반응물Ammonium fluoroborateHCID 9964072—
반응물Sodium NitriteHCID 23668193—
용매Acetic AcidHCID 176—
생성물5-bromo-1H-indazoleHCID 761929152.3%

반응 조건

온도0 °C

반응 단계

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 20) as a tan solid. The crude material was used without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07135575B2
출처 데이터셋uspto-grants-2006_11
ORD IDord-592d58f685e648b5ae6ba08bec33a139
출처 메모uspto-grants-2006_11