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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 233238Erstellt: 26. Oktober 2026

Chloroacetonitrile → HCID 178511314, Verbindung

https://huagongshe.com/reaction/233238

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktChloroacetonitrileHCID 7856—
EduktSodium BicarbonateHCID 516892—
EduktDichloromethane ethylacetateHCID 21226138—
EduktHCID 178505426HCID 178505426—
LösungsmittelAcetonitrileHCID 6342—
ProduktHCID 178511314HCID 17851131489,1%

Reaktionsschritte

To a stirred suspension of 4-(6-fluoro-1 H-indazol-3-yl)piperidine (4.95 g, 22.6 mmol) and NaHCO3 (2.1 g, 24.9 mmol) in dry acetonitrile (110 ml) was added chloroacetonitrile (1.6 ml, 24.9 mmol) at room temperature, under nitrogen. The suspension was warmed to reflux for 22.5 hours, cooled to room temperature, and subsequently filtered. The remaining solids were washed with DCM and the combined filtrates were concentrated. The resulting brown oil was dissolved into EtOAc and washed with water. The organic phase was dried (MgSO4), filtered and concentrated to give a brown solid which was re-dissolved into DCM/EtOAc and flushed through alumina with DCM. The eluent was concentrated to give 5.2 g of the desired product as a solid, m.p. 149°-151 ° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05591745
Quelldatensatzuspto-grants-1997_01
ORD IDord-e6adffb630f54654a760c85785b315d9
Quellennotizuspto-grants-1997_01