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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2367138생성일: 2026년 10월 27일

Trifluoroacetic acid → 5-Chloro-3-iodo-2-methylaniline

https://huagongshe.com/reaction/2367138

반응식

참여 물질

역할이름HCID투입량
반응물Trifluoroacetic acidHCID 6422—
반응물1,1-Dimethylethyl (5-chloro-3-iodo-2-methylphenyl)carbamateHCID 86617520—
용매DichloromethaneHCID 6344—
생성물5-Chloro-3-iodo-2-methylanilineHCID 2472920784%

반응 단계

To a solution of 1,1-dimethylethyl (5-chloro-3-iodo-2-methylphenyl)carbamate (5 g, 13.6 mmol) in dichloromethane (50 mL) was added trifluoroacetic acid (10 mL). The solution was stirred at ambient temperature for 2 hours, then concentrated in-vacuo. The resultant residue was partitioned between saturated sodium bicarbonate and ethyl acetate. The aqueous portion was extracted twice with ethyl acetate. The combined organic portions were washed with brine, dried over sodium sulfate, filtered and concentrated in-vacuo to afford an orange residue which was purified by column chromatography (silica gel, 5% ethyl acetate in hexane). The product was isolated to afford 3.05 g, 11.4 mmol (84%) of 5-chloro-3-iodo-2-methylaniline as a yellow solid. 1H NMR (400 MHz, CDCl3): 7.26 (d, 1H), 6.64 (d, 1H), 3.78 (br s, 2H), 2.28 (s, 3H); MS (EI) for C7H7Cl1N: 268 (MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08697737B2
출처 데이터셋uspto-grants-2014_04
ORD IDord-8e9dac0c98d840399d69a8542c6a9630
출처 메모uspto-grants-2014_04