HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1642109Generated: November 4, 2026
Methanol → 1-(4-Methoxybenzyl)piperidine-4-carboxaldehyde
https://huagongshe.com/reaction/1642109
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Reactant | HCID 60704011 | HCID 60704011 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1-(4-Methoxybenzyl)piperidine-4-carboxaldehyde | HCID 17893930 | — |
Reaction Steps
A 1.5 M solution of diisobutylaluminium hydride in toluene (3.12 ml, 4.68 mmol) was added dropwise under argon at −78° C., in the course of 30 minutes, to a solution of methyl 1-(4-methoxybenzyl)piperidine-4-carboxylate (1.23 g, 4.68 mmol) in toluene (30 ml), and stirring was then carried out for 30 min at that temperature. Methanol (15 ml) was then added dropwise in such a manner that the internal temperature remained at −78° C., before the mixture was then slowly warmed to room temperature. Saturated sodium chloride solution (20 ml) was added to the reaction mixture, and the suspension was filtered through sea sand. The organic phase was dried over sodium sulfate and concentrated in vacuo. The residue was purified by flash chromatography with cyclohexane/ethyl acetate (1:3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08119633B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-4f6801374b354cfeb584e65828f6e94b |
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| Source note | uspto-grants-2012_02 |
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