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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1257980생성일: 2026년 10월 27일

Water → 5-Bromo-4,4'-didodecyl-2,2'-bithiophene

https://huagongshe.com/reaction/1257980

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물N-bromobutanimideHCID 67184—
반응물4,4'-Didodecyl-2,2'-bithiopheneHCID 21917265—
용매Acetic acid chloroformHCID 21584526—
생성물5-Bromo-4,4'-didodecyl-2,2'-bithiopheneHCID 6712082085%

반응 조건

온도0 °C

반응 단계

To a solution of 4,4′-didodecyl-2,2′-bithiophene (0.100 g, 0.199 mmol) in CHCl3/HOAc (1:1) (Vt=2.0 mL) at 0° C. was added N-bromosuccimide (NBS, 35.7 mg, 0.199 mmol) in portions over a period of 45 minutes. The reaction mixture was stirred for 1 hour at 0° C. and overnight at room temperature. The reaction mixture was poured into water (50.0 mL) and extracted with chloroform (3×50.0 mL). The combined organic phases were washed with water (50.0 mL), NaOH solution, and dried over MgSO4. After filtration through Celite, the filtrate was concentrated in vacuo and the residue was purified by column chromatography on silica gel (hexanes) to provide 5-bromo-4,4′-didodecyl-2,2′-bithiophene (29A) as a colorless oil (98.0 mg, 85% yield). 1H NMR (CDCl3): δ 0.84-1.54 (m, 46H), 2.57 (m, 4H), 6.81 (s, 1H), 6.84 (s, 1H), 6.94 (s, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호USRE044304E1
출처 데이터셋uspto-grants-2013_06
ORD IDord-76cd16eac47841e4bc50a1a442274da4
출처 메모uspto-grants-2013_06