HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → 1-Ethynyl-4-iodobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (4-Iodophenylethynyl)trimethylsilane | HCID 11808725 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-Ethynyl-4-iodobenzene | HCID 12160833 | 64.8% |
Reaction Steps
To a solution of ((4-iodophenyl)ethynyl)trimethylsilane (5) (2.07 g, 6.23 mmol) in methanol (40 mL) was added K2CO3 (8.0 g, 57.9 mmol) and the reaction was allowed to stir for 48 hours. The volatiles were then removed in vacuo and the residue partitioned between ethyl acetate and H2O. The layers were separated and the aqueous phase re-extracted with ethyl acetate (2×). The combined organic layers were washed (H2O, brine), dried (Na2SO4), and filtered. The solvent was removed in vacuo and the residue was crystallized from hexane at −20° C. (in 2 crops) to give 1-ethynyl-4-iodobenzene (6) as a colorless solid (0.92 g, 64%). 1H NMR (400 MHz, DMSO-d6) δ 7.66 (app d, J=8.6 Hz, 2H), 7.20 (app d, J=8.5 Hz, 2H), 1.54 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07741347B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-b4dda8d4d4954a57bf5cb0599e52ff3b |
| Source note | uspto-grants-2010_06 |