Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | HCID 131723888 | HCID 131723888 | — |
| Catalyst | Iridium | HCID 23924 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 131723887 | HCID 131723887 | 87.4% |
Reaction Steps
Iridium complex (1,5-cyclooctadiene bis(methyldiphenylphosphine)iridium hexafluorophosphate, 112 mg, 0.096 mmol) was suspended in tetrahydrofuran (5 mL), and activated by stirring under H2 flow. To this solution, Compound 5 (864 mg, 0.95 mmol) dissolved in tetrahydrofuran (5 mL) was added, and the mixture was stirred at room temperature for 2 hours under argon gas flow. Then, iodine (484 mg), water (24.7 mL) and tetrahydrofuran (15 mL) were added thereto, and the mixture was further stirred at room temperature for 2 hours. The reaction mixture was diluted with chloroform, and washed successively with saturated sodium thiosulfate solution, saturated aqueous sodium hydrogencarbonate, and saturated brine. The chloroform layer was dried over magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (toluene:EtOAc=5:2) to obtain Compound 6 (686.6 mg, 87.1%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06562954B1 |
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| Source dataset | uspto-grants-2003_05 |
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| ORD ID | ord-6cafa2a4157340ae9f2c3ee3d401517b |
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| Source note | uspto-grants-2003_05 |
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