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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 131370생성일: 2026년 10월 26일

Nitric Acid → 3-Bromo-2-nitro-benzo(b)thiophene

https://huagongshe.com/reaction/131370

반응식

참여 물질

역할이름HCID투입량
반응물Nitric AcidHCID 944—
반응물Ethyl AcetateHCID 8857—
반응물Benzo(b)thiophene, 3-bromo-HCID 123250—
용매DichloromethaneHCID 6344—
용매Trifluoroacetic acidHCID 6422—
생성물3-Bromo-2-nitro-benzo(b)thiopheneHCID 297050—

반응 조건

온도0 °C

반응 단계

Add dropwise fuming nitric acid (90%, 8.6 mL, 183 mmol) to a mixture of 3-bromo benzo[b]thiophene (39 g, 183 mmol) in TFA (100 mL) and dichloromethane (400 mL) at 0° C. The reaction turn greenish, then yellow precipitates. To this reaction mixture, add dichloromethane (200 mL) and the reaction stir at 0° C. for 30 min. Then pour the reaction into ice-water (2L). Extract with dichloromethane (3×500 mL) and the organic layer dry over MgSO4. Evaporation give a yellow solid. The resulting yellow solid triturate with diethyl ether to give a yellow solid. (Total: 34.8 g, 73%). Mass spectrum (m/e): 259(M+1); 1HNMR(300 MHz, DMSO-d6) δ ppm: 7.70(tt, 2H), 8.04(d, 1H), 8.17(d, 1H). 13CNMR(75 MHz, DMSO-d6) δ ppm: 112.5, 124.8, 126.9, 127.9, 131.3, 137.0, 137.2, 166.1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07384934B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-80b4adacaad34e8898a241a418330c09
출처 메모uspto-grants-2008_06