HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1292123Generated: October 30, 2026
Di-tert-butyl dicarbonate → HCID 18914284, compound
https://huagongshe.com/reaction/1292123
Participants
| Role | Name | HCID | Charge |
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| Reactant | Di-tert-butyl dicarbonate | HCID 90495 | — |
| Reactant | Benzyl 2-methyl-4-oxo-3,4-dihydropyridine-1(2H)-carboxylate | HCID 11459227 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 18914284 | HCID 18914284 | 20.9% |
Reaction Steps
A mixture of 1.1 g of the crude 2(R,S)-methyl-1(benzyloxycarbonyl)-2,3-dihydro-4-pyridone, 200 mL of ethyl acetate, 1 g of di-tert-butyldicarbonate and 1 g of 10% palladium on carbon was shaken under 55 psi of hydrogen for 24 h. The mixture was filtered, concentrated under reduced pressure, and purified by low pressure chromatography on silica gel eluting with 40% ethyl acetate in hexane. There was obtained first 0.20 g of (±)-1-(2,2-dimethylethoxycarbonyl)-2-methyl-4-oxopiperidine: 1H NMR (400 MHz, CDCl3) 4.65 (m, 1H), 4.2 (m, 1H), 3.3 (m, 1H), 2.65 (dd, 1H), 2.45 (m, 1H), 2.3 (m, 1H), 2.2 (dd, 1H), 1.45 (s, 9H), 1.14 (d, 3H). Later fractions gave 0.50 g of the (±)-1-(2,2-dimethylethoxycarbonyl)-2-methyl-4-hydroxypiperidine: 1H NMR (400 MHz, CDCl3) 4.3 (m, 1H), 4.15 (t, 1H), 3.8 (m, 1H), 3.25 (m, 1H), 2.15 (s, 1H), 2.8 (m, 1H), 1.65 (m, 3H), 1.42 (s, 3H), 1.25 (d, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05756508 |
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| Source dataset | uspto-grants-1998_05 |
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| ORD ID | ord-df522161a0c04627a65240b915a7976b |
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| Source note | uspto-grants-1998_05 |
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