HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 270038Erstellt: 27. Oktober 2026
Water → 1'-benzyl-5-methyl-3H-spiro[1-benzofuran-2,4'-piperidine]
https://huagongshe.com/reaction/270038
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | Dimethylformamide | HCID 6228 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | 1-Benzyl-4-(2-fluoro-5-methylbenzyl)piperidin-4-ol | HCID 59833635 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | 1'-benzyl-5-methyl-3H-spiro[1-benzofuran-2,4'-piperidine] | HCID 59833633 | 41% |
Reaktionsschritte
To a suspension of NaH (55% in mineral oil, 200 mg, 5 mmol) in toluene (10 mL) was slowly added a solution of crude 1-benzyl-4-(2-fluoro-5-methylbenzyl)piperidin-4-ol in toluene (15 mL). After addition was completed, the reaction mixture was heated to 110° C. and stirred for 5 min. DMF (9 mL) was added and stirring was continued at reflux temperature for 10 h. The reaction mixture was cooled to room temperature, poured into water (50 ml), and extracted with ethyl acetate (2×25 ml). The organic layer was dried over Na2SO4, filtered and concentrated. The residue was purified by silica gel flash chromatography (ethyl acetate/n-heptane) to give the subtitle compound (240 mg, 41%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US07449475B2 |
|---|
| Quelldatensatz | uspto-grants-2008_11 |
|---|
| ORD ID | ord-260f62b0aab84857b4fdc4e95d4293a3 |
|---|
| Quellennotiz | uspto-grants-2008_11 |
|---|