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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1384974Erstellt: 26. Oktober 2026

4-Toluenesulfonyl chloride → (R)-3-tosyloxymethyl-1-methylpiperidine

https://huagongshe.com/reaction/1384974

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Toluenesulfonyl chlorideHCID 7397—
Edukt(R)-(1-methylpiperidin-3-yl)methanolHCID 920113—
LösungsmittelDichloromethaneHCID 6344—
Produkt(R)-3-tosyloxymethyl-1-methylpiperidineHCID 1589522242,3%

Reaktionsschritte

A solution of (R)-3-hydroxymethyl-1 -methylpiperidine (2.6 g, 20 mmol) in dichloromethane (70 mL) was cooled to 5° C. and tosyl chloride (3.8 g, 20 mmol) was added in portions during 15 minutes. After the addition was complete, the reaction was allowed to warm to room temperature and was stirred for 20 hours. The reaction mixture was then concentrated and the residue partitioned between 10% potassium hydroxide (50 mL) and ether (100 mL). The ether layer was removed and the aqueous phase extracted once again with ether (50 mL). The combined ether layers were dried over magnesium sulfate and concentrated to afford (R)-3-tosyloxymethyl-1 -methylpiperidine as a white solid (2.4 g, 42%), m.p. 74.5-81.0° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06262078B1
Quelldatensatzuspto-grants-2001_07
ORD IDord-109302689e704cf1a2f324624ab9d0fb
Quellennotizuspto-grants-2001_07