HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1472500Generated: October 29, 2026
Tetrahydrofuran → Methyl 4-chloro-3-(2-(4-fluorophenyl)ethynyl)benzoate
https://huagongshe.com/reaction/1472500
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 1-Ethynyl-4-fluorobenzene | HCID 522627 | — |
| Reactant | Methyl 4-chloro-3-iodobenzoate | HCID 15521790 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | Methyl 4-chloro-3-(2-(4-fluorophenyl)ethynyl)benzoate | HCID 70654480 | — |
Reaction Steps
Under an inert atmosphere of nitrogen, a mixture of methyl 4-chloro-3-iodobenzoate (200 mg, 0.68 mmol, 1.00 equiv), 1-ethynyl-4-fluorobenzene (243 mg, 2.02 mmol, 3.00 equiv), Pd(PPh3)2Cl2 (94.6 mg, 0.14 mmol, 0.20 equiv), CuI (13 mg, 0.07 mmol, 0.10 equiv), tetrahydrofuran (12 mL), and triethylamine (4 mL) was stirred overnight at 70° C. in an oil bath. The solids were filtered out, and the filtrate was concentrated in vacuo. The residue was purified via silica gel column chromatography (ethyl acetate/petroleum ether (1:100)) resulting in 130 mg (67%) of methyl 4-chloro-3-(2-(4-fluorophenyl)ethynyl)benzoate as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09012637B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-f908cedb16ff46909627573389de1d69 |
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| Source note | uspto-grants-2015_04 |
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