HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1837957Generated: November 3, 2026
4-Fluorophenyl 2-thienyl ketone → (4-Fluorophenyl)(2-thienyl)methanol
https://huagongshe.com/reaction/1837957
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Fluorophenyl 2-thienyl ketone | HCID 68479 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (4-Fluorophenyl)(2-thienyl)methanol | HCID 10987480 | — |
Reaction Steps
To a solution of 2-(4-fluorobenzoyl)thiophene (5.09 g, 24.7 mmol) in Et2O (100 mL) was added a solution of LiAlH4 (1M in THF, 30 mL, 30 mmol) and the reaction mixture was stirred overnight. The resulting mixture was cooled to 0° C., poured onto ice, extracted with Et2O, dried (Na2SO4) and concentrated under reduced pressure to give (4-fluorophenyl)-2-thienylmethan-1-ol as a yellow oil. The crude product was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06784167B2 |
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| Source dataset | uspto-grants-2004_08 |
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| ORD ID | ord-570da4342e30423b8dc7efde5d17f5b9 |
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| Source note | uspto-grants-2004_08 |
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