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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 390739Generated: October 23, 2026

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

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

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, 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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08383660B2
Source datasetuspto-grants-2013_02
ORD IDord-63ad3bc616ff479fa3780317a102f092
Source noteuspto-grants-2013_02