HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 745633Generated: October 30, 2026
Ethanol → 2-(4-Fluorophenyl)-2-methylbutyl alcohol
https://huagongshe.com/reaction/745633
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol | HCID 702 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 2-(4-Fluorophenyl)-2-methylbutanoic acid | HCID 13711781 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(4-Fluorophenyl)-2-methylbutyl alcohol | HCID 15582650 | 93.3% |
Reaction Steps
A solution of 3.0 g of 2-(4-fluorophenyl)-2-methylbutyric acid in 10 ml of tetrahydrofuran was added dropwise to a mixture of 20 ml of tetrahydrofuran and 0.5 g of lithium aluminum hydride at 40° C. The temperature was then elevated and the mixture was refluxed for 30 minutes. The mixture was cooled to room temperature and ethanol was added dropwise to the mixture to decompose excessive lithium aluminum hydride. Then, water was added to the mixture to complete the decomposition. The formed precipitate was removed by filtration and tetrahydrofuran was removed from the filtrate by distillation under reduced pressure. The residue was extracted with benzene, and the benzene extract was washed with water, dried over Na2SO4, and evaporated under reduced pressure to give 2.6 g of 2-(4-fluorophenyl)-2-methylbutyl alcohol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04599362 |
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| Source dataset | uspto-grants-1986_07 |
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| ORD ID | ord-3fbdfeb6f00a47859f5552fc34b23d24 |
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| Source note | uspto-grants-1986_07 |
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