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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 750953Generated: November 1, 2026

Dimethylformamide → 5-(4-(4-Methoxy-phenyl)-butyl)-2H-tetrazole

https://huagongshe.com/reaction/750953

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium AzideHCID 33557—
Reactant1-Hex-5-ynyl-4-methoxy-benzeneHCID 23614535—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product5-(4-(4-Methoxy-phenyl)-butyl)-2H-tetrazoleHCID 23614553—
ProductHCID 178490075HCID 178490075—

Reaction Steps

A mixture of 1.80 g (9.56 mmol) 1-hex-5-ynyl-4-methoxy-benzene, 1.86 g (28.6 mmol) sodium azide, 1.53 g (28.6 mmol) ammonium chloride and 80 ml DMF was kept at 125° C. for 7 d with an extra addition of 1.80 g sodium azide and 1.53 g ammonium chloride every day. After cooling to r.t. the dark reaction mixture was distributed between water and ethyl acetate. The organic phase was dried over sodium sulphate and the solvent distilled off. The residue was separated by HPLC on a RP18-endcapped column (methanol/water) (a reversed phase column PUROSPHER® STAR RP-18 endcapped from Merk KGaA, Darmstadt, Germany, which is used with methanol/water as eluent) to yield 450 mg 5-(4-(4-Methoxy-phenyl)-butyl)-2H-tetrazole and 500 mg 4-(4-(4-Methoxy-phenyl)-butyl)-1H-[1,2,3]triazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07405231B2
Source datasetuspto-grants-2008_07
ORD IDord-fe2f587ef61d4b6e918ac6fedc3f74c2
Source noteuspto-grants-2008_07