HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 522865Generated: October 31, 2026
Dimethylformamide dimethyl acetal → tert-butyl 3-[(dimethylamino)methylene]-4-oxotetrahydro-1(2H)-pyridinecarboxylate
https://huagongshe.com/reaction/522865
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide dimethyl acetal | HCID 78373 | — |
| Reactant | tert-Butyl 4-oxopiperidine-1-carboxylate | HCID 735900 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | tert-butyl 3-[(dimethylamino)methylene]-4-oxotetrahydro-1(2H)-pyridinecarboxylate | HCID 53395404 | 76% |
Reaction Steps
DMF dimethyl acetal (5.82 mL, 0.044 mol) was added to a stirred solution of tert-butyl 4-oxopiperidine-1-carboxylate (8.73 g, 0.044 mol) in DMF (80 mL) and the reaction mixture was heated to 80° C. under N2 for 18 h. After cooling, the DMF was removed under reduced pressure and the residue was partitioned between EtOAc and H2O. The organic layer was washed with H2O and saturated brine, then dried over MgSO4 and evaporated to afford tert-butyl 3-((dimethylamino)methylene)-4-oxopiperidine-1-carboxylate (8.44 g, 76%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09334269B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-24c435952cd441cea073367e5e17047c |
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| Source note | uspto-grants-2016_05 |
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