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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 644560Generated: October 30, 2026

Propargyl alcohol → HCID 67486242, compound

https://huagongshe.com/reaction/644560

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl alcoholHCID 7859—
ReactantAmmonium ChlorideHCID 25517—
Reactant7-Iodo-1-phenyl-5-(trifluoromethyl)-1H-benzimidazoleHCID 19426024—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventPyrrolidineHCID 31268—
ProductHCID 67486242HCID 67486242183.4%

Reaction Conditions

Temperature75 °C

Reaction Steps

To a stirred solution of 7-iodo-1-phenyl-5-trifluoromethylbenzimidazole (9.7 g, 25 mmol) and tetrakis (triphenylphosphine)palladium(0) (2.9 g, 5 mmol) in pyrrolidine (75 ml) was added a solution of 2-propyn-1-ol (5.6 g, 0.1 mol) in pyrrolidine (75 ml), then copper (I) iodide (475 mg, 2.5 mmol). The resulting solution was heated to 75° C. with stirring under nitrogen. After 5 h the reaction mixture was allowed to cool, treated with saturated aqueous ammonium chloride and extracted with diethyl ether. The combined organic extracts were dried over anhydrous sodium sulphate and the solvent removed under reduced pressure to leave a residue (14.5 g). This residue was flash chromatographed over silica gel (eluted with dichloromethane/diethyl ether 4:1) to give the desired product (2.53 g, 32%) m/z, 316.8 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07700638B2
Source datasetuspto-grants-2010_04
ORD IDord-3bd7213e7eb54c63bd5187fc597e87a0
Source noteuspto-grants-2010_04