HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2266882Generated: November 2, 2026
HCID 10442110, compound → HCID 86001735, compound
https://huagongshe.com/reaction/2266882
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 10442110 | HCID 10442110 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 86001735 | HCID 86001735 | 55% |
Reaction Steps
A solution of LAH (2.74 g, 72.3 mmol) in Et2O (230 mL) was stirred under nitrogen at 0° C. 2-Ethyl-4,4,4-trifluorobutyric acid (12.3 g, 72.3 mmol) in Et2O (20 mL) was added dropwise, and the solution stirred for 15 min at 0° C. and then 2 h at 25° C. After this time period, the solution was quenched with the dropwise addition of H2O (2.74 mL), 15% NaOH (2.74 mL), and H2O (8.22 mL) with efficient stirring. Solid Na2SO4 was added to dry the solvent, and the resulting mixture was stirred for 1 h. The resulting slurry was filtered, and the filter cake washed with excess Et2O. After concentration, the crude product was purified by the Biotage Flash™ 40 chromatography instrument, eluent: 20:80 to 30:70 Et2O:PE to obtain 2-ethyl-4,4,4-trifluorobutanol as an oil (6.18 g, 55% yield for two steps).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07858658B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-a5f322f358ea48c09fd9f74e04a255c8 |
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| Source note | uspto-grants-2010_12 |
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