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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 840680Erstellt: 25. Oktober 2026

Dimethyl Sulfate → N-Boc-2-Methyl-Piperidine

https://huagongshe.com/reaction/840680

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethyl SulfateHCID 6497—
EduktN,N,N',N'-TetramethylethylenediamineHCID 8037—
EduktN-(tert-butoxycarbonyl)piperidineHCID 7010304—
EduktCID 53628100HCID 178418400—
LösungsmittelWaterHCID 962—
LösungsmittelDiethyl EtherHCID 3283—
ProduktN-Boc-2-Methyl-PiperidineHCID 457807799,2%

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

A solution of N-Boc-Piperidine (15.0 g, 80.95 mmol) in ether (160 mL) was cooled to −78° C. and treated with TMEDA (15.9 mL, 105.2 mmol) followed by sec-BuLi (85 mL, 105.2 mmol) dropwise. The mixture was stirred for 3 h at −78° C. and then treated with a solution of dimethyl sulfate (15.3 mL, 161.9 mmol) in 65 mL of ether. The mixture was warmed to room temperature and then was diluted with water and extracted with ether. The combined extracts were dried over K2CO3 and then concentrated to give a crude product as a colorless oil. The product was purified by column chromatography on silca gel with 5% EtOAc/hexane to afford 16.0 g (81%) of product as a clear oil which was homogeneous by TLC analysis. 1H NMR (300 MHz) 67 4.33 (m, 1 H), 3.92-3.81 (pair of br. d, 1 H), 2.81-2.72 (dt, 1H), 1.60-1.36 (m, 15 H), 1.09-1.07 (d, 3 H); 13C NMR (75 MHz) 154.9 (s), 78.6 (s), 45.9 (s), 38.6 (s), 29.9 (s), 28.4 (s), 25.6 (s), 18.6 (s), 15.6 (s), ppm.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06369078B1
Quelldatensatzuspto-grants-2002_04
ORD IDord-04bcec3d8e0849d38352a346ae5610cd
Quellennotizuspto-grants-2002_04