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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1386742Generated: November 2, 2026

Ethyl orthoformate → 1-((4-methoxyphenyl)methyl)-1H-1,2,3,4-tetrazole

https://huagongshe.com/reaction/1386742

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl orthoformateHCID 31214—
ReactantSodium AzideHCID 33557—
Reactant4-MethoxybenzylamineHCID 75452—
SolventAcetic AcidHCID 176—
Product1-((4-methoxyphenyl)methyl)-1H-1,2,3,4-tetrazoleHCID 1099780543.6%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 3.84 g (28.0 mmol) of (4-methoxy)benzylamine, 2.73 g (42.0 mmol) of sodium azide and 7.50 mL (45.0 mmol) triethyl orthoformate in 25 mL of HOAc was stirred at 80° C. for 20 h. The reaction was cooled and concentrated. The residue was partitioned between 100 mL of EtOAc and 100 mL of H2O and the layers were separated. The organic layer was washed with 100 mL of 2.0 N HCl, 100 mL of sat'd NaHCO3, 100 mL of sat'd NaCl, dried over MgSO4 and concentrated. Flash chromatography on 100 g of silica gel using 2:1 v/v hexanes/EtOAc, then 1:1 v/v hexanes/EtOAc as the eluant afforded 2.32 g of the title compound: 1H NMR (300 MHz) δ 3.82 (s, 3H), 5.53 (s, 2H), 6.93 (d, J=8.6, 2H), 7.27 (d, J=8.6, 2H), 8.46 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06265434B1
Source datasetuspto-grants-2001_07
ORD IDord-4f3df1f3124e413c9b4bc171c0423abb
Source noteuspto-grants-2001_07