Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Diisobutylaluminum hydride | HCID 14487 | — |
| Reactant | Potassium bisulfate | HCID 516920 | — |
| Reactant | HCID 68823916 | HCID 68823916 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68826125 | HCID 68826125 | 105.6% |
Reaction Steps
Within 15 min was dropped 1.46 ml (1.2 M in toluene, 1.75 mmol) of DIBAL-H to a dry ice cooled (−30° C.) solution of 0.23 g (0.88 mmol) 6-(4-trifluoromethoxy-phenyl)-hex-5-yn-2-one in 4 ml of THF. The reaction was warmed up (0° C. for 1 h 10 min) and neutralized with aqueous 10% KHSO4 solution. The mixture was extracted with ether (three times), the organic phases were washed with a aqueous 10% NaCl solution, dried (Na2SO4) and evaporated to give 0.24 g of the title compound as light brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07253192B2 |
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| Source dataset | uspto-grants-2007_08 |
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| ORD ID | ord-45472b325b314324aa0113fffbc1db61 |
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| Source note | uspto-grants-2007_08 |
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