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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol | HCID 702 | — |
| Reactant | 3,5-Bis(trifluoromethyl)benzaldehyde | HCID 136247 | — |
| Reactant | 2-methyl-2H-1,2,3,4-tetrazol-5-amine | HCID 138677 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 5-[N-(3',5'-Bistrifluoromethylbenzyl)amino]-2-methyltetrazole | HCID 23073221 | 87.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08383660B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-63ad3bc616ff479fa3780317a102f092 |
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| Source note | uspto-grants-2013_02 |
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