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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1050965Erstellt: 26. Oktober 2026

Hydrochloric Acid → Tert-butyl 4-(4-formylphenyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/1050965

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktDiethylsilaneHCID 68337—
EduktTert-butyl 4-[4-(methoxycarbonyl)phenyl]-1-piperidinecarboxylateHCID 22492933—
KatalysatorChlorobis(cyclooctene)iridium(I) dimerHCID 91972094—
LösungsmittelDichloromethaneHCID 6344—
ProduktTert-butyl 4-(4-formylphenyl)piperidine-1-carboxylateHCID 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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09388142B2
Quelldatensatzuspto-grants-2016_07
ORD IDord-a2d39eaebcff4592a102c56034108187
Quellennotizuspto-grants-2016_07