HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 453908Generated: October 30, 2026
Methanol → Benzyl 4-formylpiperidine-1-carboxylate
https://huagongshe.com/reaction/453908
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Diisobutylaluminum hydride | HCID 14487 | — |
| Reactant | HCID 86188531 | HCID 86188531 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Benzyl 4-formylpiperidine-1-carboxylate | HCID 2776272 | — |
Reaction Steps
A solution of 1-benzyl 4-methylpiperidine-1,4-dicarboxylate (10 g) in toluene (100 ml), under nitrogen, was cooled to −78° C. Then DIBAL-H (60.9 ml) was added dropwise at −78° C., and the mixture was stirred for 1 h at that temperature (TLC monitoring). Because the reaction was incomplete, a further 0.2 eq. of DIBAL-H was added and stirring was carried out for a further 30 min (TLC monitoring: some starting material and the corresponding alcohol were detectable). Methanol (40 ml) followed by sat. sodium chloride solution (40 ml) were added slowly to the reaction mixture at −78° C. The mixture was filtered over celite, and the solvent was removed under vacuum. The residue was extracted with ethyl acetate (3×75 ml), dried (Na2SO4) and concentrated under vacuum. The crude product so obtained was purified by column chromatography (silica gel, 20% ethyl acetate/hexane). Yield: 4.3 g (49%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08492559B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-45d598a0f01d49a68f90abaa3bc8556f |
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| Source note | uspto-grants-2013_07 |
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