HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → Methyl 4-(piperidin-4-yl)-1-naphthoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1-Chloroethyl chloroformate | HCID 521305 | — |
| Reactant | Methyl 4-(1-methylpiperidin-4-yl)-1-naphthoate | HCID 22711881 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 4-(piperidin-4-yl)-1-naphthoate | HCID 22711878 | 88% |
Reaction Steps
A solution of D9 (0.39 g, 1.4 mmole) in DCM (30 ml) was treated with iPr2EtN (0.26 g, 2 mmole) followed by 1-chloroethyl chloroformate (0.29 g, 2 mmole) and stirred at room temperature for 3 h, then concentrated under vacuum and the residue treated with MeOH (30 ml) and heated under reflux for 1 h. The mixture was allowed to cool and the solid filtered off, washed with Et2O and dried. This was treated with 10% Na2CO3 solution, extracted with DCM and the extract dried and concentrated under vacuum to afford the title compound as a colourless oil (0.33 g, 88%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06747030B1 |
| Source dataset | uspto-grants-2004_06 |
| ORD ID | ord-b50637576bef4526889503b437468e8b |
| Source note | uspto-grants-2004_06 |