HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 41342Erstellt: 25. Oktober 2026
Ethyl ketone → 7,7,7-Trifluoro-3-ethyl-3-heptanol
https://huagongshe.com/reaction/41342
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Ethyl ketone | HCID 7288 | — |
| Edukt | 4-Bromo-1,1,1-trifluorobutane | HCID 521006 | — |
| Edukt | Magnesium | HCID 5462224 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 7,7,7-Trifluoro-3-ethyl-3-heptanol | HCID 86640092 | 76,1% |
Reaktionsschritte
1.3 g of magnesium, 10.0 g of 1-bromo-4,4,4-trifluorobutane and 20 g of tetrahydrofuran were added to a four-necked flask equipped with a nitrogen feeding pipe, a reflux condenser, a dropping funnel and a thermometer, and a Grignard reagent was prepared by a conventional method. Then, a mixture containing 5.0 g of 3-pentanone and 4 g of tetrahydrofuran was dropwise added to the obtained Grignard reagent at a temperature of 25 to 35° C. over 30 minutes, followed by stirring at the same temperature for 1 hour. The reaction mixture was treated by a conventional method, and the resulting organic phase was washed with water, followed by drying with anhydrous magnesium sulfate. Thereafter, the resultant was concentrated under reduced pressure, thereby obtaining 7.9 g of 7,7,7-trifluoro-3-ethyl-3-heptanol in the form of a pale yellow oily matter.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08530598B2 |
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| Quelldatensatz | uspto-grants-2013_09 |
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| ORD ID | ord-606d302f54874402afc4c8a6e2f4cb8d |
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| Quellennotiz | uspto-grants-2013_09 |
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