HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1253670Generated: November 2, 2026
Methanol → Benzyl 4-formylpiperidine-1-carboxylate
https://huagongshe.com/reaction/1253670
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Diisobutylaluminum hydride | HCID 14487 | — |
| Reactant | 1-Benzyl 4-methyl piperidine-1,4-dicarboxylate | HCID 1512544 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Benzyl 4-formylpiperidine-1-carboxylate | HCID 2776272 | — |
Reaction Steps
A solution of 1-benzyl 4-methyl piperidine-1,4-dicarboxylate (10 g) in toluene (100 ml) under nitrogen was cooled to −78° C. DIBAL-H (60.9 ml) was then added dropwise at −78° C. and the mixture was stirred at this temperature for 1 h (TLC control). Because the reaction was incomplete, a further 0.2 eq. of DIBAL-H was added and the mixture was stirred for a further 30 min (TLC control: some educt and the corresponding alcohol were to be detected). 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 in vacuo. The residue was extracted with ethyl acetate (3×75 ml) and the extract was dried (Na2SO4) and concentrated in vacuo. The crude product obtained in this way 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 | US08455475B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-ff57934744c34703992b7aa2f1b5c1c2 |
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| Source note | uspto-grants-2013_06 |
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