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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1073233Generated: October 30, 2026

Hydrochloric Acid → HCID 178441193, compound

https://huagongshe.com/reaction/1073233

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium AzideHCID 33557—
ReactantTriethylazanium chlorideHCID 12698378—
ReactantHCID 19987804HCID 19987804—
SolventWaterHCID 962—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 178441193HCID 17844119341.4%

Reaction Conditions

Temperature150 °C

Reaction Steps

Under a nitrogen atmosphere, a mixture of 7.00 g (0.023 mole) of 5-(3,5-di-t-butyl-4-hydroxyphenoxy)-valeronitrile, 4.73 g (0.034 mole) of triethylammonium chloride, 4,47 g (0.069 mole) of sodium azide and 200 ml of 1-methylpyrrolidone was heated at 150° C. for about 60 hours. The reaction mixture was cooled and then poured into 200 ml of water. The aqueous mixture was acidified to pH 1 with 10% hydrochloric acid and then extracted five times with 100 ml portions of diethyl ether. The diethyl ether extracts were combined, washed with brine, dried over magnesium sulfate and evaporated to provide an oil. The oil was purified by silica gel chromatography eluting with 2:1 hexane:acetone containing 3 ml of acetic acid per 1600 ml of solvent followed by recrystallization of the isolated material from a mixture of ethyl acetate and hexane to provide 3.3 g of 5-[4-(3,5-di-t-butyl-4-hydroxyphenoxy)butyl]tetrazole as a white solid, m.p. 141°-141.5° C. Analysis: Calculated for C19H30N4O2 : %C, 65.9; %H, 8.7; %N, 16.2; Found: %C, 65.7; %H, 8.6; %N, 16.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04968710
Source datasetuspto-grants-1990_11
ORD IDord-5b364cf0a5d54036b48991411c616154
Source noteuspto-grants-1990_11