HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 424319Generated: October 29, 2026
Ethyl ketone → 7,7,7-Trifluoro-3-ethyl-3-heptanol
https://huagongshe.com/reaction/424319
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl ketone | HCID 7288 | — |
| Reactant | 4-Bromo-1,1,1-trifluorobutane | HCID 521006 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 7,7,7-Trifluoro-3-ethyl-3-heptanol | HCID 86640092 | 76.1% |
Reaction Steps
1.3 g of magnesium, 10.0 g of 1-bromo-4,4,4-trifluorobutane and 20 g of tetrahydrofuran were charged into a four-necked flask equipped with a nitrogen feeding tube, a reflux condenser, a dropping funnel and a thermometer, and a Grignard reagent was prepared by a conventional method. Then, a mixture of 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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08105747B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-bdb25224107a4e85b544c56d315a6230 |
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| Source note | uspto-grants-2012_01 |
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