돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1850039생성일: 2026년 10월 24일

Benzyl Bromide → 2-Benzyl-6-bromo-2H-indazole

https://huagongshe.com/ko/reaction/1850039

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl BromideHCID 7498—
반응물Ethyl AcetateHCID 8857—
반응물6-Bromo-1H-indazoleHCID 17842471—
용매1,4-DioxaneHCID 31275—
생성물2-Benzyl-6-bromo-2H-indazoleHCID 58529689—

반응 단계

6-Bromoindazole (3.63 g, 18 mmol) was suspended in dioxane (15 mL) and benzyl bromide (2.65 mL, 22 mmol, 1.2 eq.) was added. The reaction was heated to reflux overnight, then allowed to cool to 80° C. after which point ethyl acetate (50 mL) added. The cake was broken up with a spatula and after stirring for 20 min, the solids were filtered off and washed with ethyl acetate, giving glossy white crystals of the hydrobromide salt of 2-benzyl-6-bromoindazole. These were suspended in ethyl acetate (100 mL) and shaken with saturated NaHCO3 (150 mL) until dissolution. The layers were separated and the aqueous layer was extracted with ethyl acetate (50 mL). The combined organic layers were concentrated to an off-white powder which was recrystallized from 66% ethanol (40 mL). Washing with water and drying in vacuo gave 2-benzyl-6-bromoindazole (3.30 g, 62%) as shiny white plates.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08957049B2
출처 데이터셋uspto-grants-2015_02
ORD IDord-9f201dd0cce546afaab84d6a390c9720
출처 메모uspto-grants-2015_02