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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 390739생성일: 2026년 10월 23일

Ethanol → 5-[N-(3',5'-Bistrifluoromethylbenzyl)amino]-2-methyltetrazole

https://huagongshe.com/ko/reaction/390739

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물3,5-Bis(trifluoromethyl)benzaldehydeHCID 136247—
반응물2-methyl-2H-1,2,3,4-tetrazol-5-amineHCID 138677—
반응물Sodium borohydrideHCID 4311764—
용매TolueneHCID 1140—
생성물5-[N-(3',5'-Bistrifluoromethylbenzyl)amino]-2-methyltetrazoleHCID 2307322187.6%

반응 단계

A mixture of 3,5-bis(trifluoromethyl)benzaldehyde (4 g, 16.5 mmol), 2-methyl-2H-tetrazol-5-amine (1.96 g, 19.8 mmol) and molecular sieves (5-10 Å beads) in toluene (50 mL) was heated at reflux for 4 hours, after which time the solvent was removed. Ethanol (50 mL) and sodium borohydride (1.25 g, 33 mmol) were added. The resulting mixture was stirred at room temperature for 30 minutes and then partitioned between saturated NH4Cl (50 mL) and ethyl acetate (2×50 mL). The combined organic layers were washed with saturated NaCl (50 mL), dried (MgSO4), filtered and concentrated to yield the title compound as a white solid (4.7 g). 1H NMR (400 MHz, CDCl3) δ 4.2 (s, 3 H) 4.7 (s, 1 H) 4.7 (s, 1 H) 5.0 (t, J=6.0 Hz, 1 H) 7.8 (s, 1 H) 7.9 (s, 2 H). MS (ES+) Calc: 325.08, Found: 325.8 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08383660B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-63ad3bc616ff479fa3780317a102f092
출처 메모uspto-grants-2013_02