HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2247445Generated: October 31, 2026
Triethylamine → Methyl {3'-[3-(2,4-dichlorophenyl)-2-propynyloxy]-4'-methoxybiphenyl-3-yl}acetate
https://huagongshe.com/reaction/2247445
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2,4-Dichloro-1-iodobenzene | HCID 96864 | — |
| Reactant | Methyl (4'-methoxy-3'-(2-propynyloxy)biphenyl-3-yl)acetate | HCID 59218932 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Methyl {3'-[3-(2,4-dichlorophenyl)-2-propynyloxy]-4'-methoxybiphenyl-3-yl}acetate | HCID 86594837 | — |
Reaction Steps
9 mg of methyl (4′-methoxy-3′-(2-propynyloxy)biphenyl-3-yl)acetate was dissolved in 0.1 ml of N,N-dimethylformamide, 30 mg of 2,4-dichloroiodobenzene, 2 mg of copper iodide, 2 mg of tetrakistriphenyl phosphine palladium and 0.05 ml of triethylamine were added thereto, and the mixture was stirred at room temperature for 3 days. The reaction mixture was diluted with ethyl acetate and washed with water. The organic layer was concentrated to give methyl {3′-[3-(2,4-dichlorophenyl)-2-propynyloxy]-4′-methoxybiphenyl-3-yl}acetate. This product was dissolved in 0.5 ml of ethanol, then 0.1 ml of 5N sodium hydroxide was added thereto, and the mixture was left overnight at room temperature. The reaction mixture was neutralized with 1N hydrochloric acid and extracted with ethyl acetate. The organic layer was concentrated, and the residue was purified by reverse-phase high performance liquid chromatography to give 4.24 mg of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07687664B2 |
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| Source dataset | uspto-grants-2010_03 |
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| ORD ID | ord-650e5569671c45b3a81602ac9ff64696 |
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| Source note | uspto-grants-2010_03 |
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