Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 225007Generated: October 30, 2026

1H-1,2,4-Triazole → HCID 54087959, compound

https://huagongshe.com/reaction/225007

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-1,2,4-TriazoleHCID 9257—
ReactantBromineHCID 24408—
ReactantSodium hydrideHCID 24758—
Reactant4,4-Dimethyl-1-phenylpent-1-en-3-oneHCID 95494—
SolventWaterHCID 962—
SolventCarbon TetrachlorideHCID 5943—
SolventDimethylformamideHCID 6228—
ProductHCID 54087959HCID 54087959—

Reaction Steps

2,2-Dimethyl-5-phenylpent-4-ene-3-one (9.48 g) in carbon tetrachloride (60 ml) was treated dropwise with bromine (8.0 g). The solution was evaporated in a vacuum and the pale yellow residue of 4,5-dibromo-2,2-dimethyl-5-phenylpentan-3-one (12.6 g) collected. The dibromo compound so prepared (6.96 g) was dissolved in dry dimethylformamide (20 ml) and added dropwise to a mixture obtained by adding 1,2,4-triazole (2.76 g) to a suspension of sodium hydride (1.92 of 50% dispersion in mineral oil, washed free of oil with dry petrol) in dimethylformamide (10 ml). The resulting mixture was heated on a steambath for 15 minutes and poured into cold water (200 ml). The mixture was extracted with ether and the ether extracts dried and evaporated to give a pale yellow oil. This oil crystallised from petrol to give 2,2-dimethyl-5-phenyl-5-(1,2,4-triazol-1-yl)pent-4-en-3-one (compound no. 1 of Table I) having a melting point of 70°- 73° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04235620
Source datasetuspto-grants-1980_11
ORD IDord-dd6193f4059a410c947538443c5150f5
Source noteuspto-grants-1980_11