HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → Butyl 4-oxopiperidine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Piperonylamine | HCID 2723901 | — |
| Reactant | Pyrocarbonate | HCID 15238643 | — |
| Product | Butyl 4-oxopiperidine-1-carboxylate | HCID 22732029 | — |
Reaction Steps
About 2 g of 4-piperidone hydrochloride monohydrate (FIG. 10a) was dissolved in about 30 ml of N,N-dimethylformamide at temperatures of between about 110-115° C. The solution was cooled to room temperature, and to this solution was added about 2.6 g of triethyl amine and a solution containing about 3.06 g of ditertarybutyl dicarbonate in 10 ml DMF. The reaction was continued for about 24 hours at room temperature. The DMF was removed under reduced pressure. About 100 ml of water was added to the residue and the mixture was extracted with ethyl ether (2×100 ml), and the organic layer dried over anhydrous MgSO4. The ether was evaporated to dryness under reduced pressure to yield about 2.33 g of the compound of FIG. 10b.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06420370B1 |
| Source dataset | uspto-grants-2002_07 |
| ORD ID | ord-f73a84b269f4451bb2a370f803eab873 |
| Source note | uspto-grants-2002_07 |