HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 644560Generated: October 30, 2026
Propargyl alcohol → HCID 67486242, compound
https://huagongshe.com/reaction/644560
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Propargyl alcohol | HCID 7859 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 7-Iodo-1-phenyl-5-(trifluoromethyl)-1H-benzimidazole | HCID 19426024 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Pyrrolidine | HCID 31268 | — |
| Product | HCID 67486242 | HCID 67486242 | 183.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07700638B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-3bd7213e7eb54c63bd5187fc597e87a0 |
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| Source note | uspto-grants-2010_04 |
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