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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 127238Generated: October 26, 2026

1H-1,2,4-Triazole → 4-Chloro-1-(4-chlorophenoxy)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)-butan-2-one naphthalene-1,5-disulphonate

https://huagongshe.com/reaction/127238

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-1,2,4-TriazoleHCID 9257—
ReactantNaphthalenedisulfonic acidHCID 3015207—
Reactant1-Bromo-4-chloro-1-(4-chlorophenoxy)-3,3-dimethyl-butan-2-oneHCID 20286562—
SolventAcetoneHCID 180—
SolventAcetonitrileHCID 6342—
Product4-Chloro-1-(4-chlorophenoxy)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)-butan-2-one naphthalene-1,5-disulphonateHCID 20286577192.6%

Reaction Steps

268.3 g (0.79 mol) of crude 1-bromo-4-chloro-1-(4-chlorophenoxy)-3,3-dimethyl-butan-2-one were dissolved in 2 l of absolute acetonitrile. 190 g (2.7 mol) of 1,2,4-triazole were added thereto and the mixture was heated for 20 hours under reflux. It was then concentrated by distilling off the solvent in vacuo and the residue was taken up in 1,000 ml of methylene chloride. The mixture was washed three times with 250 ml of water at a time, dried over sodium sulphate and again concentrated in vacuo. The oil which remained was dissolved in 1,000 ml of acetone and a solution of 140 g (0.48 mol) of naphthalenedisulphonic acid in 500 ml of acetone was added. After 30 minutes, the resulting precipitate was filtered off. 285 g (76.6% of theory) of 4-chloro-1-(4-chlorophenoxy)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)-butan-2-one naphthalene-1,5-disulphonate of melting point 245° C. (with decomposition) were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04255434
Source datasetuspto-grants-1981_03
ORD IDord-5cb06980892b4e3e94355ccb305ed7cf
Source noteuspto-grants-1981_03