HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2295196Generated: October 30, 2026
Aluminium lithium hydride → HCID 15099539, compound
https://huagongshe.com/reaction/2295196
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | HCID 86749411 | HCID 86749411 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 15099539 | HCID 15099539 | — |
Reaction Steps
To a slurry of LiAlH4 (1.457 gm, 38.4 mmol) in dry THF at 0° C. was added a solution of 2-(4-fluorophenyl)-4-(1-methylethyl)-6-phenyl-3-pyridinecarboxylic acid, ethyl ester (3.37 gm, 9.27 mmol) in THF (7 ml). After 4.5 hours, the flask was charged with an additional 0.88 gm LiAlH4 and stirring was continued for 2 more hours. The mixture was quenched with H2O and diluted with H2O and EtOAc. The phases were shaken and separated, and the aqueous layer was extracted again with EtOAc and Et2O. The pooled organic layers were washed with H2O and brine, then dried (Na2SO4), filtered and stripped to give a white solid. The solid was recrystallized from hot EtOAc/hexane to afford 2-(4-fluorophenyl)-4-(1-methylethyl)-6-phenyl-3-pyridinemethanol as white crystals. The mother liquor was stripped and recrystallized again from hot EtOAc/hexane to give a total of 2.684 gm (90%) desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05691322 |
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| Source dataset | uspto-grants-1997_11 |
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| ORD ID | ord-2cc82299a3d440d2bee40e7be63656f4 |
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| Source note | uspto-grants-1997_11 |
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