HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 15729Erstellt: 23. Oktober 2026
Ammonium Hydroxide → Benzyl 2-(4-chlorophenyl)-4-oxopiperidine-1-carboxylate
https://huagongshe.com/de/reaction/15729
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ammonium Hydroxide | HCID 14923 | — |
| Edukt | Ammonium Chloride | HCID 25517 | — |
| Edukt | Benzyl 3,4-dihydro-4-oxo-pyridine-1(2H)-carboxylate | HCID 11368235 | — |
| Edukt | HCID 178478191 | HCID 178478191 | — |
| Edukt | HCID 178494437 | HCID 178494437 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | Benzyl 2-(4-chlorophenyl)-4-oxopiperidine-1-carboxylate | HCID 59342393 | — |
Reaktionsschritte
CuBr.SMe2 complex (1.49 g, 7.26 mmol) was added to 25 mL of anhydrous THF and cooled to −78° C. 4-Chlorophenylmagnesium bromide (7.26 mL, 1.0 M in THF, 7.26 mmol) was added slowly via syringe. Stirring at −78° C. for 1 hour produced an orange then green-like suspension. Boron trifluoride dimethyl etherate (0.92 mL, 7.26 mmol) was added and stirred for 5 minutes. To the newly formed complex was then added over 1 hour a solution of the compound 66 (1.0 g, 4.32 mmol) in 15 mL of anhydrous THF. After stirring 2 hours at −78° C., 16 mL of aq. 20% NH4Cl/conc. NH4OH (1:1) was added, and the mixture was allowed to warm-up to room temperature. EtOAc was used to extract (3×100 mL) and the combined organic layers were washed with brine and dried (MgSO4). Solvent was removed by rotary evaporation and the residue was purified by flash chromatography to give the product 67 as a colorless oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US07732609B2 |
|---|
| Quelldatensatz | uspto-grants-2010_06 |
|---|
| ORD ID | ord-ab71bfae619241b3a6352d150f024773 |
|---|
| Quellennotiz | uspto-grants-2010_06 |
|---|