HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 548550Generated: October 28, 2026
HCID 15524951, compound → HCID 67157886, compound
https://huagongshe.com/reaction/548550
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 15524951 | HCID 15524951 | — |
| Reactant | HCID 86627833 | HCID 86627833 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 67157886 | HCID 67157886 | — |
Reaction Steps
A mixture of 1,3-dibromo-5-phenylethynyl-benzene (0.1 g, 0.3 mmol, intermediate 3), (4-prop-2-ynyloxy-phenoxy)-acetic acid methyl ester (66 mg, 0.3 mmol), Pd(PPh3)2Cl2 (10 mg, 0.015 mmol), CuI (16 mg, 0.008 mmol) in dry DMF (1.5 ml) and triethylamine (1.5 ml) was heated in a microwave own for 10 min at 70° C. in a sealed tube. The reaction mixture was filtered through Decalite and the filtrate was evaporated. The residue was purified on column chromatography to give {4-[3-(3-bromo-5-phenylethynyl-phenyl)-prop-2-ynyloxy]-phenoxy}-acetic acid methyl ester in 27 mg (20%) yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07943612B2 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-0e67cbd1d51c47a7b91fdfc0df8e04d4 |
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| Source note | uspto-grants-2011_05 |
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