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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 352563생성일: 2026년 10월 25일

1,3,5-Tribromobenzene → 2-Bromo-1-(2,4,6-tribromo-phenyl)-ethanone

https://huagongshe.com/reaction/352563

반응식

참여 물질

역할이름HCID투입량
반응물1,3,5-TribromobenzeneHCID 12279—
반응물Bromoacetyl bromideHCID 61147—
반응물Chloromethyl Thienyl Ketone deriv. 5HCID 6539169—
생성물2-Bromo-1-(2,4,6-tribromo-phenyl)-ethanoneHCID 1012728545%

반응 단계

General procedure described for compounds 1 and 2 starting from 1,3,5-tribromobenzene and bromoacetyl bromide. Purified by column chromatography column (hexane:ethyl acetate 6:1), yield 45% m.p.: 86-87° C., 1H-NMR (CDCl3): δ7.7 (s, 2H, Ar), 4.44 (s, 2H, CH2); 13C-NMR (CDCl3): δ193.4 (CO), 139.4 (C—CO), 134.5 (CH), 124.7 (C—Br), 119.4 (C—Br), 34.6 (CH2); M/z (EI): 440, 438, 436, 434, 432 (M+, 1, 3, 5, 3, 1%), 345, 343, 341, 339 (M-CH2Br, 35, 96, 100, 41%); HPLC: Column μ Bondapack C18, 5 μm, 300 A, (300×3.9 mm), Purity 98%, r.t.=3.40 min, acetonitrile/H2O (0.05% H3PO4+0.04% Et3N) 50/50.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06747057B2
출처 데이터셋uspto-grants-2004_06
ORD IDord-c5e379a66aa647afbbd28357312b1007
출처 메모uspto-grants-2004_06