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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1919723Erstellt: 26. Oktober 2026

Dimethyl Sulfate → N-Boc-2-Ethyl-6-methylPiperidine

https://huagongshe.com/reaction/1919723

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethyl SulfateHCID 6497—
EduktN,N,N',N'-TetramethylethylenediamineHCID 8037—
Edukttert-Butyl 2-Ethylpiperidine-1-carboxylateHCID 12170201—
EduktCID 53628100HCID 178418400—
LösungsmittelWaterHCID 962—
LösungsmittelDiethyl EtherHCID 3283—
ProduktN-Boc-2-Ethyl-6-methylPiperidineHCID 2262014859%

Reaktionsbedingungen

Temperatur-20 °C

Reaktionsschritte

A solution of N-Boc-2-ethylpiperidine (1.5 g, 7.0 mmol) in 28 mL of ether was cooled to −60° C. and treated with TMEDA (1.6 mL, 10.85 mmol), followed by sec-BuLi (8.5 mL, 10.85 mmol) dropwise. The mixture was slowly warmed to −20° C., stirred for 30 min, and then cooled to −78° C. The mixture was treated with a solution of dimethyl sulfate (1.6 mL, 16.69 mmol) in ether and slowly warmed to room temperature. The mixture was diluted with water and then extracted with ether. The combined extracts were dried over K2CO3 and concentrated to give a crude product as an oil which was chromatographed on silica with 5% EtOAc/hexane to give 0.88 g (59%) of the product which was homogeneous by TLC analysis. 1H NMR (250 MHz) δ 3.91-3.87 (m, 1H), 3.69-3.65 (m, 1H), 1.83-1.41 (m, 17H), 1.21-1.19 (d, 3H), 0.85-0.82 (t, 3H); 13C NMR (62.7 MHz) 155.2 (s), 78.6 (s), 53.0 (s), 46.8 (s), 28.5 (s), 27.2 (s), 26.7 (s), 22.4 (s), 20.7 (s), 13.4 (s), 11.4 (s) ppm.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08168657B2
Quelldatensatzuspto-grants-2012_05
ORD IDord-a2c66eea1a8b437ea6a106e794bad348
Quellennotizuspto-grants-2012_05