HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 400664Generated: November 1, 2026
HCID 60026398, compound → HCID 60026332, compound
https://huagongshe.com/reaction/400664
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 60026398 | HCID 60026398 | — |
| Reactant | HCID 86040733 | HCID 86040733 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 60026332 | HCID 60026332 | 43% |
Reaction Steps
A mixture of trifluoromethanesulfonic acid 4-cyano-2-methyl-6-nitrophenyl ester (217 mg, 0.7 mmol), dichlorobis(triphenylphosphine)palladium (II) (24.6 mg, 0.035 mmol), copper (I) iodide (13.3 mg, 0.7 mmol), and 6-(5-methanesulfonyl-2,3-dihydrobenzofuran-7-yl)-6-methyl-4-trifluoromethylhept-1-yn-4-ol (273 mg, 0.7 mmol) in a mixture of 0.8 mL of anhydrous toluene and 0.3 mL of anhydrous triethylamine was heated in a microwave at 60° C. for 10 minutes. The reaction mixture was applied to a column of SiO2 (50% ethyl acetate in hexanes) to give 165 mg of the title product as a light yellow oil (43% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08741897B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-5c818b4ee13e4d7b80a9914bb5d2183d |
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| Source note | uspto-grants-2014_06 |
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