HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 12645Generated: October 25, 2026
Hydrochloric Acid → {4-[Dimethylamino-(3-fluorophenyl)-methyl]-cyclohexyl}-acetaldehyde
https://huagongshe.com/reaction/12645
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methoxymethyl-triphenylphosphonium chloride | HCID 2723798 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | 4-[Dimethylamino-(3-fluorophenyl)-methyl]-cyclohexane-carbaldehyde | HCID 86627888 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | {4-[Dimethylamino-(3-fluorophenyl)-methyl]-cyclohexyl}-acetaldehyde | HCID 86627887 | — |
Reaction Steps
(Methoxymethyl)triphenylphosphonium chloride (26.73 g, 78 mmole) was suspended in absolute THF (90 ml) under argon, potassium tert-butylate (8.75 g, 78 mmole), dissolved in absolute THF (90 ml), was added dropwise at 0° C., and the mixture was then stirred for 15 minutes at 0° C. The aldehyde 9b (13.69 g, 52 mmole), dissolved in absolute THF (90 ml), was then added dropwise at RT and the mixture was stirred overnight at RT. The mixture was hydrolysed by dropwise addition of water (50 ml) and 6N HCl (150 ml), while cooling with iced water. After stirring for one hour at RT the mixture was extracted 10 times with ether (each time 50 ml). The aqueous phase was adjusted to pH 11 with 5N NaOH, shaken three times with ethyl acetate (each time 100 ml), dried over Na2 SO4 and concentrated by evaporation in vacuo. The crude product was purified by flash chromatography with ethyl acetate/cyclohexane (1:1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07728028B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-cd99407096e045d89a559822721c434e |
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| Source note | uspto-grants-2010_06 |
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