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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 483113Generated: October 28, 2026

Iodine → HCID 13259985, compound

https://huagongshe.com/reaction/483113

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantPropargyl bromideHCID 7842—
ReactantAmmonium ChlorideHCID 25517—
ReactantAluminumHCID 5359268—
ReactantHCID 13259981HCID 13259981—
CatalystMercuric ChlorideHCID 24085—
SolventTetrahydrofuranHCID 8028—
ProductHCID 13259985HCID 1325998574.8%

Reaction Conditions

Temperature-60 °C

Reaction Steps

1.58 g (0.058 mol) of aluminum (in the form of flakes) are covered with a layer of 7.3 ml of tetrahydrofuran, and a catalytic amount (0.05 g) of mercury(II) chloride and an iodine crystal are added. After the mixture has stood for 12 hours at 20° C., 10.3 g (0.087 mol) of propargyl bromide in 11 ml of tetrahydrofuran are added dropwise at 60° C. The mixture is then cooled to -60° C., and a solution of 17.1 g (0.05 mol) of 5-(2,4-dichlorophenoxy)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)pentan-2-one in 20 ml of tetrahydrofuran is added dropwise. The mixture is allowed to warm up to 0° C. and is kept for a further hour at this temperature, and 22 ml of a saturated, aqueous ammonium chloride solution are added. Thereafter, the mixture is filtered, the filtrate is evaporated down in vacuo and the residue is taken up in 200 ml of ethyl acetate. After the solution has been washed with three times 100 ml of water, the organic phase is dried over sodium sulphate and then evaporated down in vacuo. Residues of solvent are removed at 50° C. and 0.01 mbar. 14.3 g (74.8% of theory) of 7-(2,4-dichlorophenoxy)-5,5-dimethyl-4-(1,2,4-triazol-1-yl-methyl)-hept-1-in-4-ol are obtained as a brownish oil of refractive index nD20 =1.5642.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04578396
Source datasetuspto-grants-1986_03
ORD IDord-8581513d304c4e70beb2dd859e76000d
Source noteuspto-grants-1986_03