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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1263261Generated: October 26, 2026

Water → 2,2-Dimethyl-8-phenoxy-4-(1H-1,2,4-triazol-1-yl)octan-3-one

https://huagongshe.com/reaction/1263261

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant(4-Bromobutoxy)benzeneHCID 70986—
Reactant3,3-Dimethyl-1-(1H-1,2,4-triazol-1-yl)-2-butanoneHCID 100877—
SolventDimethylformamideHCID 6228—
Product2,2-Dimethyl-8-phenoxy-4-(1H-1,2,4-triazol-1-yl)octan-3-oneHCID 12806674—

Reaction Steps

A solution of 14.3 g of 2,2-dimethyl-4-(1,2,4-triazol-1-yl)-butan-3-one (cf. German Laid-Open Application DOS No. 2,638,470) in 20 ml of dimethylformamide was added dropwise, under a dry nitrogen atmosphere, to a stirred suspension of 2.3 g of sodium hydride in 20 ml of dimethylformamide, the reaction temperature being kept at 20°-30° C. by cooling; the mixture was subsequently stirred for 20 hours at room temperature. A solution of 19.5 g of 1-bromo-4-phenoxybutane in 20 ml of dimethylformamide was then added dropwise at 5°-10° C., with continued stirring, and while cooling with ice. After completion of the addition, stirring was continued for 10 hours at 5°-10° C., after which 200 ml of water were added and the mixture was extracted with twice 100 ml of methylene chloride. The combined organic phases were extracted by shaking with water and dried over magnesium sulfate; removal of the solvent under reduced pressure gave an oil from which, on trituration with 20 ml of diisopropyl ether, 17 g of colorless crystals were precipitated; melting point 59°-62° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04456608
Source datasetuspto-grants-1984_06
ORD IDord-d894d7a47e744e04896956335a083720
Source noteuspto-grants-1984_06