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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 262452Generated: October 29, 2026

1H-1,2,4-Triazole → HCID 23350019, compound

https://huagongshe.com/reaction/262452

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-1,2,4-TriazoleHCID 9257—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 21319211HCID 21319211—
Reactant1,5-Naphthalenedisulphonic acid octahydrateHCID 86736531—
SolventAcetoneHCID 180—
ProductHCID 23350019HCID 2335001970.3%

Reaction Steps

A solution of 36.3 g (0.2 mol) of crude 4-acetoxy-1-bromo-1-(4-chlorophenoxy)-3,3-dimethyl-butan-2-one in 50 ml of acetone was added dropwise, at the boil, to a suspension of 21 g (0.3 mol) of 1,2,4-triazole and 30g (0.2 mol) of potassium carbonate in 200 ml of acetone. After heating for 15 hours under reflux, the mixture was filtered and the filtrate was concentrated by distilling off the solvent in vacuo. The residue was taken up in 200 ml of methylene chloride and the solution was washed three times with 50 ml of water at a time, dried over sodium sulphate and concentrated. The residue was dissolved in 100 ml of acetone and 36 g (0.1 mol) of 1,5-naphthalenedisulphonic acid octahydrate in 100 ml of acetone were added. The crystalline precipitate which resulted was filtered off and dried. 45 g (45% of theory) of 4-acetoxy-1-(4-chloro-phenoxy)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)-butan-2-one 1,5-naphthalenedisulphonate of melting point 155°-160° C. were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04154842
Source datasetuspto-grants-1979_05
ORD IDord-2de565b740bc4da19c8048d8ebc84e84
Source noteuspto-grants-1979_05