HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2116612Generated: November 2, 2026
Dimethylformamide dimethyl acetal → 478623-90-4
https://huagongshe.com/reaction/2116612
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide dimethyl acetal | HCID 78373 | — |
| Reactant | Di-tert-butyl dicarbonate | HCID 90495 | — |
| Reactant | tert-Butyl 3,5-dioxopiperidine-1-carboxylate | HCID 21942204 | — |
| Product | 478623-90-4 | HCID 68928249 | 99% |
Reaction Steps
56.0 g (of 1,1-dimethylethyl 3,5-dioxo-1-piperidinecarboxylate having the empirical formula C10H15NO4 (prepared by a method similar to that described in Heterocycles, 22, 2769-2773, (1984), replacing methyl chloroformate with (BOC)2O, are prepared as a suspension. 55.5 ml of N,N-dimethylformamide dimethyl acetal at 95% are added at room temperature. The medium is stirred for half an hour at 80° C. and then for 3 hours at 50° C. The solvent is evaporated off under reduced pressure. 79 g of 1,1-dimethylethyl 4-[(dimethylamino)methylene]-3,5-dioxo-1-piperidinecarboxylate having the empirical formula C13H20N2O4 are thus obtained. The corresponding yield is 99%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07439253B2 |
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| Source dataset | uspto-grants-2008_10 |
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| ORD ID | ord-9d93656102e340efbdcd4ace57f4c2e1 |
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| Source note | uspto-grants-2008_10 |
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