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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 330378Generated: October 30, 2026

Ammonium Chloride → 5-[[3-(2-Phenyl-4-thiazolylmethoxy)phenyl]methyl]-1H-tetrazole

https://huagongshe.com/reaction/330378

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium AzideHCID 33557—
Reactant3-(2-Phenyl-4-thiazolylmethoxy)benzenacetonitrileHCID 14479985—
ReactantEthyl acetate hexaneHCID 21226206—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product5-[[3-(2-Phenyl-4-thiazolylmethoxy)phenyl]methyl]-1H-tetrazoleHCID 17842015529%

Reaction Conditions

Temperature135 °C

Reaction Steps

To a solution of 9.0 g (0.03 mol) of 3-(2-phenyl-4-thiazolylmethoxy)benzenacetonitrile in 200 ml of dimethylformamide are added 9.5 g (0.15 mol) of sodium azide and 7.9 g (0.15 mol) of ammonium chloride, and the slurry is heated to 135° C. for 72 hours. The mixture is allowed to cool to room temperature, diluted with 200 ml of water, and extracted four times with 200 ml of ethyl acetate. The combined ethyl acetate solution is washed with brine, dried over anhydrous magnesium sulfate, and concentrated in vacuo to obtain an oil, which is subjected to high pressure liquid chromatography (ethyl acetate/hexane as eluent). Fraction 2 is concentrated to obtain 3.0 g (29%) of crystals, m.p. 160°-161° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04895953
Source datasetuspto-grants-1990_01
ORD IDord-88f773cb2c604fd989dc71c87669930c
Source noteuspto-grants-1990_01