HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Morpholine → (4-(4-Methylpiperidin-1-yl)-3-nitrophenyl)methanol
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Morpholine | HCID 8083 | — |
| Edukt | 4-Methylpiperidine | HCID 69381 | — |
| Edukt | 4-Fluoro-3-nitrobenzyl alcohol | HCID 4167587 | — |
| Lösungsmittel | Chloroform | HCID 6212 | — |
| Produkt | (4-(4-Methylpiperidin-1-yl)-3-nitrophenyl)methanol | HCID 28963353 | — |
Reaktionsbedingungen
| Temperatur | 50 °C |
|---|
Reaktionsschritte
A stirred suspension of (4-fluoro-3-nitro-phenyl)-methanol (171 mg, 1 mmol), 4-methyl piperidine (95 mg, 0.96 mmol) PS morpholine (400 mg, 1 mmol), and chloroform (3 mL) was heated at 50° C. for 2 hrs. The reaction was evaporated onto celite and purified by flash chromatography to give [4-(4-methyl-piperidin-1-yl)-3-nitro-phenyl]-methanol (i). 1H NMR (CDCl3, 300 MHz): δ 7.8 (s, 1H), 7.4 (d, 1H), 7.1 (d, 1H), 4.6 (s, 2H), 3.2 (d, 2H), 2.8 (dd, 2H), 1.8-1.3 (m, 5H), 1.0 (d, 3H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07790724B2 |
| Quelldatensatz | uspto-grants-2010_09 |
| ORD ID | ord-002306e905e14ec69694e607e23c2a70 |
| Quellennotiz | uspto-grants-2010_09 |