HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2293828Generated: October 31, 2026
Aluminium lithium hydride → HCID 14460147, compound
https://huagongshe.com/reaction/2293828
Participants
| Role | Name | HCID | Charge |
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| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | HCID 86749408 | HCID 86749408 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 14460147 | HCID 14460147 | 66% |
Reaction Steps
A slurry of LiAlH4 (305 mg, 8.04 mmol) in dry Et2O (30 ml) at 0° C. treated with a solution of 4-(4-fluorophenyl)-2-methyl-6-phenyl-3-pyridinecarboxylic acid, ethyl ester (1.587 gm, 4.73 mmol) in Et2O (4 ml). After 50 minutes, the reaction was quenched and diluted with H2O and the solution was adjusted to neutral pH with 10% HCl. EtOAc was added to dissolve suspended product into the Et2O layer and the mixture was subsequently extracted three times with EtOAc. The combined organic layers were washed with H2O and brine, then dried (Na2SO4), filtered and stripped to give a yellow solid. Recrystallization of the solid from hot hexane/acetone afforded 4-(4-fluorophenyl)-2-methyl-6-phenyl-3-pyridinemethanol (916 mg) as a white solid. An additional 283 mg of 4-(4-fluorophenyl)-2-methyl-6-phenyl-3-pyridinemethanol was obtained by evaporation of the mother liquor followed by recrystallization of the residue from hot hexane/EtOAc, giving a total of 1.199 gm (86%) product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05686433 |
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| Source dataset | uspto-grants-1997_11 |
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| ORD ID | ord-54405f70b6774cd990002fa240a94bd5 |
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| Source note | uspto-grants-1997_11 |
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