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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2166352Generated: October 30, 2026

Iodine → HCID 13259988, compound

https://huagongshe.com/reaction/2166352

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantPropargyl bromideHCID 7842—
ReactantAmmonium ChlorideHCID 25517—
ReactantAluminumHCID 5359268—
Reactant1-(4-Chlorophenyl)-4,4-dimethyl-2-(1H-1,2,4-triazol-1-yl)-3-pentanoneHCID 12925561—
CatalystMercuric ChlorideHCID 24085—
SolventTetrahydrofuranHCID 8028—
ProductHCID 13259988HCID 1325998874.2%

Reaction Conditions

Temperature60 °C

Reaction Steps

3.7 g of aluminum (in the form of flakes), a pinch of mercury(II) chloride and an iodine crystal are stirred with 20 ml of absolute tetrahydrofuran for 12 hours. 24 g (0.2 mol) of propargyl bromide, dissolved in 25 ml of tetrahydrofuran, are then added dropwise at 50° to 60° C. The mixture is stirred for a further 30 minutes at 60° C. and cooled to -60° C., and 29.2 g (0.1 mol) of 5-(4-chlorophenyl)-2,2-dimethyl-4-(1,2,4-triazol-1-yl)-pentan-3-one in 100 ml of tetrahydrofuran are slowly added dropwise. Thereafter, the reaction mixture is stirred for a further hour at 0° C. and for 2 hours at 20° C., 50 ml of saturated, aqueous ammonium chloride solution are added, while cooling, the mixture is filtered and the filtrate is evaporated down. The remaining crystalline residue is digested with water and recrystallized from 520 ml of cyclohexane. 24.6 g (74.2% of theory) of 4-tert.-butyl-6-(4-chlorophenyl)-5-(1,2,4-triazol-1-yl)-hex-1-in-4-ol of melting point 121° C. are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04945101
Source datasetuspto-grants-1990_07
ORD IDord-0e6f63a2bb064495959e44101569993d
Source noteuspto-grants-1990_07