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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 390739Erstellt: 24. Oktober 2026

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

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolHCID 702—
Edukt3,5-Bis(trifluoromethyl)benzaldehydeHCID 136247—
Edukt2-methyl-2H-1,2,3,4-tetrazol-5-amineHCID 138677—
EduktSodium borohydrideHCID 4311764—
LösungsmittelTolueneHCID 1140—
Produkt5-[N-(3',5'-Bistrifluoromethylbenzyl)amino]-2-methyltetrazoleHCID 2307322187,6%

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08383660B2
Quelldatensatzuspto-grants-2013_02
ORD IDord-63ad3bc616ff479fa3780317a102f092
Quellennotizuspto-grants-2013_02