Reaktion #1138147

ord-a2d39eaebcff4592a102c56034108187

Reaktionsgleichung

COC(=O)c1ccc(C2CCN(C(=O)OC(C)(C)C)CC2)cc1
4-(4-methoxycarbonyl-phenyl)-piperidine-1-carboxylic acid tert-butyl ester
CC[SiH2]CC
diethylsilane
Cl
hydrochloric acid
CC(C)(C)OC(=O)N1CCC(c2ccc(C=O)cc2)CC1
4-(4-formyl-phenyl)-piperidine-1-carboxylic acid tert-butyl ester

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigethe mixture is irradiated in a microwave reactor for 1.5 hours at 50° C
  2. 2
    SonstigeThe organic layer is separated
  3. 3
    Trocknendried over sodium sulfate
  4. 4
    Sonstigeevaporated
  5. 5
    SonstigeThe residue is chromatographed on a silica gel column with cyclohexane/ethyl acetate as eluent

Vorschrift

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.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09388142B2uspto-grants-2016_07