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HRID 390739作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物3,5-Bis(trifluoromethyl)benzaldehydeHCID 136247—
反応物2-methyl-2H-1,2,3,4-tetrazol-5-amineHCID 138677—
反応物Sodium borohydrideHCID 4311764—
溶媒TolueneHCID 1140—
生成物5-[N-(3',5'-Bistrifluoromethylbenzyl)amino]-2-methyltetrazoleHCID 2307322187.6%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08383660B2
出典データセットuspto-grants-2013_02
ORD IDord-63ad3bc616ff479fa3780317a102f092
出典メモuspto-grants-2013_02