Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1,2,4,5-Tetraiodobenzene | HCID 12488 | — |
| Reactant | 4-Pentyn-1-ol | HCID 79346 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | triethylamine N,N-dimethylformamide | HCID 22056947 | — |
| Product | HCID 57733963 | HCID 57733963 | — |
Reaction Steps
To a degassed solution of 1,2,4,5-tetraiodobenzene (5.81 g, 0.01 mol) in DMF-Et3N (100 mL, 1:1) were added Pd(PPh3)2Cl2 (350 mg. 0.5 mmol), CuI (200 mg, 1.2 mmol), and 4-pentyn-1-ol (4.2 g, 0.05 mol) was added drop-wise. The mixture was stirred under N2 at room temperature for 24 h. The solution was poured into water (400 mL). The mixture was extracted with CH2Cl2 (3×200 mL). The combined organic phases were washed with 5% HCl and brine, dried over Na2SO4, and concentrated under vacuum. The residue was purified by silica gel column chromatography using CH2Cl2-MeOH (10:1, v/v) as eluent to afford tetramer (3.34 g, 82%): 1H NMR (300 MHz, CD3Cl+CO3OD δ ppm), 7.30 (s, 2H), 3.72 (t, J=6.3 Hz, 8H), 2.52 (t, J=7.2 Hz, 8H), 1.80 (p, J=6.6 Hz, 8H) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08629163B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-e9198c8f91f8468f95de0a1f3576891b |
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| Source note | uspto-grants-2014_01 |
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