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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 490857생성일: 2026년 10월 25일

2-Bromothiophene → HCID 86078978, 화합물

https://huagongshe.com/reaction/490857

반응식

참여 물질

역할이름HCID투입량
반응물2-BromothiopheneHCID 13851—
반응물Pentafluorobenzoyl chlorideHCID 75256—
반응물Aluminum(III) ChlorideHCID 6451240—
용매Carbon DisulfideHCID 6348—
생성물HCID 86078978HCID 8607897833.3%

반응 단계

To a mixture of perfluorobenzoyl chloride (2.51 g, 10.9 mmol) and 2-bromothiophene (1.86 g, 11.4 mmol) in carbon disulfide (80 mL), aluminum chloride (2.90 g, 21.8 mmol) was added in portions over 10 min with vigorous mechanical stirring. The reaction mixture turned red and was stirred for 2.5 h before being quenched with water (80 mL). The organics were then separated, the aqueous layer extracted with carbon disulfide (3×50 mL), and the combined organics washed with water (3×100 mL) and dried over MgSO4. After filtration, the organics were concentrated in vacuo and the chromatographed on a silica gel column (hexane:ether=9:1) to yield 1.23 g (32%) green crystals. mp 51-54° C.; 1H NMR (DMSO): δ 7.78 (d, 2H, 3J=3.6 Hz), 7.54 (d, 2H, 3J=4.4 Hz); 19F NMR (DMSO): δ −142.1 (m, 2H), −151.6 (m, 1H), −160.6 (m, 2H) Anal. Calcd for C11H2BrF5OS: C 37.00, H 0.56. Found: C 37.37, H 0.83; MS (EI): m/z (%) 355.8 (92) [M+].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07528176B2
출처 데이터셋uspto-grants-2009_05
ORD IDord-3755f55c2b0f42b1aaa99adce2ebf18f
출처 메모uspto-grants-2009_05