HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 619622Generated: October 30, 2026
Ethyl 4-iodobenzoate → HCID 10150285, compound
https://huagongshe.com/reaction/619622
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl 4-iodobenzoate | HCID 142891 | — |
| Reactant | HCID 21957876 | HCID 21957876 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 10150285 | HCID 10150285 | 72.2% |
Reaction Steps
A solution of 6-ethynyl-2,2-dimethylthiochroman-4-one (Compound 222, 82.0 mg, 0.38 mmol) and ethyl 4-iodobenzoate (104.9 mg, 0.38 mmol) in 5.0 mL Et3N was purged with argon for 10 minutes. To this solution were added bis(triphenylphosphine)-palladium(II) chloride (88.0 mg, 0.12 mmol) and copper(I) iodide (22.9 mg, 0.12 mmol). After sparging for an additional 5 minutes with argon, the solution was stirred overnight at room temperature. The reaction mixture was filtered through a pad of Celite using an Et2O wash. Concentration of the filtrate under reduced pressure, followed by column chromatography of the residual solid, afforded 100 mg (72%) of the title compound as a yellow solid. 1H NMR (300 MHz, CDCl3) δ: 8.25 (1H, d, J=1.8 Hz), 8.00 (2H, d, J=8.4 Hz), 7.55 (2H, d, J=8.4 Hz), 7.53 (1H, dd, J=1.8, 8.2 Hz), 7.21 (1H, d, J=8.2 Hz), 4.37 (2H, q, J=7.1 Hz), 2.88 (2H, s), 1.47 (6H, s), 1.39 (3H, t, J=7.1 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05958954 |
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| Source dataset | uspto-grants-1999_09 |
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| ORD ID | ord-87db53cf82b54403a79719379bb9d7dd |
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| Source note | uspto-grants-1999_09 |
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