HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1807910Generated: October 29, 2026
Aluminium lithium hydride → 4-(4-Fluoro-phenyl)-4-methyl-pentanal
https://huagongshe.com/reaction/1807910
Participants
| Role | Name | HCID | Charge |
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| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | 4-(4-Fluoro-phenyl)-4-methyl-pentanoic acid methoxy-methyl-amide | HCID 86638533 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(4-Fluoro-phenyl)-4-methyl-pentanal | HCID 86638534 | — |
Reaction Steps
To a solution of 4-(4-fluoro-phenyl)-4-methyl-pentanoic acid methoxy-methyl-amide (3.90 g) in tetrahydrofuran (70 ml) at −30° C. was added dropwise over 10 min a suspension of lithium aluminum hydride in tetrahydrofuran (15.4 ml, 1 M suspension). The mixture was stirred for a further 30 min at −30° C. and then cooled to −78° C. The mixture was quenched by dropwise addition of acetone (25 ml) and the mixture was then allowed to warm to room temperature. The mixture was then diluted with water and taken up in ethyl acetate. The mixture was washed sequentially with 1 N aq. hydrochloric acid and with saturated brine, then dried over Na2SO4 and concentrated in vacuo. The residue was purified by column chromatography (SiO2, heptane/EtOAc gradient) to yield a colourless oil, (1.62 g, 54%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08357712B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-2d50488b6b5e4571a24fe741f7727cb5 |
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| Source note | uspto-grants-2013_01 |
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