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HRID 1919771Erstellt: 26. Oktober 2026
Lithium Hydroxide → 5-[4-[1,1,1,3,3,3-Hexafluoro-2-(methoxymethyl)oxypropan-2-yl]-2-propylphenyloxy]pentan-2-ol
https://huagongshe.com/reaction/1919771
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Lithium Hydroxide | HCID 3939 | — |
| Edukt | 5-[4-[1,1,1,3,3,3-Hexafluoro-2-(methoxymethyl)oxypropan-2-yl]-2-propylphenyloxy]pent-2-yl acetate | HCID 59235133 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | 5-[4-[1,1,1,3,3,3-Hexafluoro-2-(methoxymethyl)oxypropan-2-yl]-2-propylphenyloxy]pentan-2-ol | HCID 59235034 | 93,2% |
Reaktionsschritte
A 2 mol/L Lithium hydroxide solution (2 mL) was added to a mixed solution of 5-[4-[1,1,1,3,3,3-hexafluoro-2-(methoxymethyl)oxypropan-2-yl]-2-propylphenyloxy]pent-2-yl acetate (80.4 mg, 169 μmol) in methanol (1.5 mL) at room temperature, followed by heating at an external temperature of 60° C. in an oil bath overnight. After completion of the reaction, methanol was evaporated under reduced pressure. The pH was adjusted to 7 by adding 4 mol/L hydrochloric acid (2 mL) to the residue. After extraction with chloroform-water, the organic layer was washed with a saturated sodium chloride solution and dried over sodium sulfate. After filtration, the filtrate was concentrated under reduced pressure. 68.1 mg of the title compound (yield: 93%) was obtained as a colorless oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08168666B2 |
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| Quelldatensatz | uspto-grants-2012_05 |
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| ORD ID | ord-243e2e93a5bf448ea8f5dd45ebf866c0 |
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| Quellennotiz | uspto-grants-2012_05 |
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