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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 976773Generated: October 29, 2026

Chloroacetonitrile → HCID 178511314, compound

https://huagongshe.com/reaction/976773

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 numberUS05612342
Source datasetuspto-grants-1997_03
ORD IDord-f12ca8ba71d44edba9fa612c7663cb8c
Source noteuspto-grants-1997_03