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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2198766Generated: October 31, 2026

Acetonitrile → HCID 12899882, compound

https://huagongshe.com/reaction/2198766

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
Reactant3,3-Bis-fluoromethyl-1-bromo-1-(4-chlorophenoxy)-butan-2-oneHCID 13019436—
ReactantHCID 178418936HCID 178418936—
ProductHCID 12899882HCID 1289988271%

Reaction Conditions

Temperature50 °C

Reaction Steps

190 g (0.557 mol) of 3,3-bisfluoromethyl-1-bromo-1-(4-chlorophenoxy)-butan-2-one and 90 g (1.3 mols) of triazole were introduced into 800 ml of acetonitrile, the mixture was heated at 50° C. for 5 hours, the solvent was distilled off under a waterpump vacuum, the residue was taken up in one liter of methylene chloride and washed twice with 1,000 ml of water each time, the organic phase was dried over sodium sulphate and the solvent was distilled off. The residue was taken up in 500 ml of diisopropyl ether and the precipitate was filtered off. The mother liquor was distilled. 130.5 g (71% of theory) of 3,3-bisfluoromethyl-1-(4-chlorophenoxy)-1-(1,2,4-triazol-1-yl)-butan-2-one of boiling point 160°-66° C./0.2 mm Hg were obtained. ##STR76##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04359470
Source datasetuspto-grants-1982_11
ORD IDord-5ded20473a3d43a1b42bed03d4f8c101
Source noteuspto-grants-1982_11