Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2075015Generated: October 30, 2026

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

https://huagongshe.com/reaction/2075015

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant3,5-Bis(trifluoromethyl)benzaldehydeHCID 136247—
Reactant2-methyl-2H-1,2,3,4-tetrazol-5-amineHCID 138677—
ReactantSodium borohydrideHCID 4311764—
SolventTolueneHCID 1140—
Product5-[N-(3',5'-Bistrifluoromethylbenzyl)amino]-2-methyltetrazoleHCID 2307322187.6%

Reaction Steps

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, 3H) 4.7 (s, 1H) 4.7 (s, 1H) 5.0 (t, J=6.0 Hz, 1H) 7.8 (s, 1H) 7.9 (s, 2H). MS (ES+) Calc: 325.08, Found: 325.8 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07919506B2
Source datasetuspto-grants-2011_04
ORD IDord-474a6ce6c1b243d784b8bd19c7230d45
Source noteuspto-grants-2011_04