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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 587782생성일: 2026년 10월 25일

Ammonia → 4-Bromo-3,5-dichlorobenzaldehyde

https://huagongshe.com/reaction/587782

반응식

참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물Tert-Butyl nitriteHCID 10906—
반응물Methyl 4-amino-3,5-dichlorobenzoateHCID 604808—
반응물4-Bromo-3,5-dichloro-benzoic acid methyl esterHCID 50849686—
용매AcetonitrileHCID 6342—
생성물4-Bromo-3,5-dichlorobenzaldehydeHCID 22421097—

반응 단계

Methyl 4-bromo-3,5-dichlorobenzoate: CuBr2 (7.5 g, 34.08 mmol) in MeCN (50 mL) was stirred at 80° C. for 30 min. To this solution tert-butylnitrite (6.5 mL, 54.55 mmol) was added dropwise at the same temperature and the mixture was stirred for another 10 min. Methyl 4-amino-3,5-dichlorobenzoate in MeCN (30 mL) was added dropwise to the reaction mixture which was then stirred at 80° C. for 30 min. The reaction mixture was brought to ambient temperature. Aqueous ammonia solution (20 mL) was added and extracted with petroleum ether. The organic layer was washed with brine followed by water. The organic solution was dried (Na2SO4), filtered and concentrated to afford the title compound as an off white solid (7.5 g, 77%): 1H NMR (300 MHz, DMSO-d6) δ 8.02 (s, 2H), 3.94 (s, 3H); ESIMS m/z 282 ([M]+); IR (thin film) 1733, 762, 514 cm−1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09226501B2
출처 데이터셋uspto-grants-2016_01
ORD IDord-c5bd742776c54ec0a7ffe5bcc619d108
출처 메모uspto-grants-2016_01