HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 52449Generated: October 28, 2026
Ethyl 4-iodobenzoate → HCID 19963736, compound
https://huagongshe.com/reaction/52449
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl 4-iodobenzoate | HCID 142891 | — |
| Reactant | 4,4-Dimethyl-2-isopropoxy-1,2,3,4-tetrahydro-7-ethynylquinoline | HCID 19963706 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Diethylamine | HCID 8021 | — |
| Product | HCID 19963736 | HCID 19963736 | — |
Reaction Steps
To a solution of 0.097 g (0.40 mmol) of 4,4-dimethyl-2-isopropoxy-1,2,3,4-tetrahydro-7-ethynylquinoline (Compound 27) and 1.16 g (0.75 ml, 4.2 mmol) of ethyl 4-iodobenzoate in 3.0 ml of diethylamine which was degassed under argon for 15 min, was added 0.043 g (0.23 mmol) of copper(I) iodide and then 0.064 g (0.09 mmol) of bis(triphenylphosphine)palladium(II) chloride. The reaction was stirred at room temperature for 16 h. The reaction mixture was then concentrated. Purification by flash chromatography (1.5% EtOAc in hexane) gave the title compound as an oil. PNMR (CDCl3) d 8.00 (2H, d, J=8.2 Hz), 7.54 (2H, d, J=8.1 Hz), 7.32 (1H, s), 7.23 (2H, s), 5.40 (1H, p, J=6.3 Hz), 4.37 (2H, q, J=7.1 Hz), 2.24 (2H, s), 1.39 (3H, t, J=7.1 Hz), 1.32 (6H, d, J=6.2 Hz), 1.24 (6H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05616712 |
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| Source dataset | uspto-grants-1997_04 |
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| ORD ID | ord-da262a4a015e4cd1ac42e7bfcd61d789 |
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| Source note | uspto-grants-1997_04 |
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