HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Hydrochloric Acid → Tert-butyl 4-(4-formylphenyl)piperidine-1-carboxylate
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Diethylsilane | HCID 68337 | — |
| Edukt | Tert-butyl 4-[4-(methoxycarbonyl)phenyl]-1-piperidinecarboxylate | HCID 22492933 | — |
| Katalysator | Chlorobis(cyclooctene)iridium(I) dimer | HCID 91972094 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | Tert-butyl 4-(4-formylphenyl)piperidine-1-carboxylate | HCID 11254770 | — |
Reaktionsschritte
To a solution of 4-(4-methoxycarbonyl-phenyl)-piperidine-1-carboxylic acid tert-butyl ester (776 mg, 2.43 mmol) in dichloromethane (10 ml) are added diethylsilane (470 μl, 3.64 mmol) and chlorobis(cyclooctene)iridium(I) dimer (22 mg, 0.025 mmol) and the mixture is irradiated in a microwave reactor for 1.5 hours at 50° C. The reaction mixture is stirred vigorously with 2 N hydrochloric acid (0.6 ml) for 30 minutes. The organic layer is separated, dried over sodium sulfate and evaporated. The residue is chromatographed on a silica gel column with cyclohexane/ethyl acetate as eluent to afford 4-(4-formyl-phenyl)-piperidine-1-carboxylic acid tert-butyl ester as yellow resin; HPLC/MS 2.10 min (A), [M-tBu] 234.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US09388142B2 |
| Quelldatensatz | uspto-grants-2016_07 |
| ORD ID | ord-a2d39eaebcff4592a102c56034108187 |
| Quellennotiz | uspto-grants-2016_07 |