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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2075040생성일: 2026년 10월 27일

3,5-Bis(trifluoromethyl)benzaldehyde → N-(2-Bromo-4-methyl-5-(trifluoromethyl)benzyl)(3,5-bis(trifluoromethyl)phenyl)methanamine

https://huagongshe.com/reaction/2075040

반응식

참여 물질

역할이름HCID투입량
반응물3,5-Bis(trifluoromethyl)benzaldehydeHCID 136247—
반응물Sodium BicarbonateHCID 516892—
반응물Sodium bis(acetyloxy)boranuidyl acetateHCID 23676153—
반응물Benzenemethanamine, 2-bromo-4-methyl-5-(trifluoromethyl)-HCID 58968640—
용매TolueneHCID 1140—
용매Ethyl AcetateHCID 8857—
생성물N-(2-Bromo-4-methyl-5-(trifluoromethyl)benzyl)(3,5-bis(trifluoromethyl)phenyl)methanamineHCID 5896872898.4%

반응 단계

A mixture of (2-bromo-4-methyl-5-(trifluoromethyl) phenyl) methanamine (189 mg, 0.705 mmol) and 3,5 bistrifluoromethyl benzaldehyde (170 mg, 0.705 mmol) in anhydrous toluene (10 mL) was heated under reflux for 3 hours. The solvent was removed under reduced pressure and the residue was dissolved in dichloromethane (25 mL). Sodium triacetoxyborohyride (373.5 mg, 1.76 mmol) was added and the mixture was stirred for 18 hours at room temperature. The mixture was poured into a mixture of saturated NaHCO3 (50 mL) and ethyl acetate (50 mL) and stirred for 30 minutes. The layers were separated and the aqueous layer was extracted with ethyl acetate (2×50 mL). The combined organic layer was dried with anhydrous sodium sulfate, filtered and concentrated to give the title compound (98.4%). 1H NMR (400 MHz, CDCl3) δ 7.83 (s, 2H) 7.76(s, 1H) 7.58(s, 1H) 7.41 (s, 1H) 3.92(s, 2H) 3.89(s, 2H) 2.44(s, 3H)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07919506B2
출처 데이터셋uspto-grants-2011_04
ORD IDord-c6127e5008244144bd721a51c9cefc98
출처 메모uspto-grants-2011_04