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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1451004Generated: October 30, 2026

Chloroacetonitrile → HCID 178511314, compound

https://huagongshe.com/reaction/1451004

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetonitrileHCID 7856—
ReactantSodium BicarbonateHCID 516892—
ReactantDichloromethane ethylacetateHCID 21226138—
ReactantHCID 178505426HCID 178505426—
SolventAcetonitrileHCID 6342—
ProductHCID 178511314HCID 17851131489.1%

Reaction Steps

To a stirred suspension of 4-(6-fluoro-1H-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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05602158
Source datasetuspto-grants-1997_02
ORD IDord-02e5b865dc344de6ab1aba5424945c70
Source noteuspto-grants-1997_02