HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromopropane → 1-Isopropylpiperidin-4-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromopropane | HCID 6358 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Piperidin-4-ol | HCID 79341 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-Isopropylpiperidin-4-ol | HCID 79681 | 80% |
Reaction Steps
4-Hydroxypiperidine (2.13 g, 21.1 mmol), K2CO3 (5.83 g, 2 eq.), 2-bromopropane (11.2 g, 91 mmol, 4.3 eq.) and MeOH (21.3 ml) were refluxed together overnight. The reaction was allowed to cool to room temperature and quenched with 2M HCl solution (40 ml) and extracted with TBME (40 ml). The aqueous phase was basified to pH 14 with 2M NaOH solution and extracted with DCM (9×50 ml). The combined organic extracts were dried over MgSO4, filtered, washed with DCM and concentrated in vacuo to give 1-isopropyl-4-hydroxypiperidine (2.41 g, 80%) as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07456164B2 |
| Source dataset | uspto-grants-2008_11 |
| ORD ID | ord-b0b76fbc78e1415187f5e84fbb8f54b7 |
| Source note | uspto-grants-2008_11 |