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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1953842Generated: November 4, 2026

Chloroacetone → HCID 23298223, compound

https://huagongshe.com/reaction/1953842

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetoneHCID 6571—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 15541113HCID 15541113—
CatalystPotassium IodideHCID 4875—
SolventAcetoneHCID 180—
ProductHCID 23298223HCID 23298223116.5%

Reaction Conditions

Temperature60 °C

Reaction Steps

The title B compound of Example 1, 4'-hydroxy-[1,1'-biphenyl]-2-carbonitrile (3.00 g, 15.4 mmol) was dissolved in acetone (8 mL) and chloroacetone (1.59 mL, 20.0 mmol), freshly ground potassium carbonate (2.12 g, 15.4 mmol) and potassium iodide (128 mg, 0.77 mmol) were added. The mixture was heated to 60° C. for 15 hours then partitioned between hydrochloric acid (1.0 M) and ethyl acetate. The aqueous phase was extracted with ethyl acetate and the combined organic extracts dried over magnesium sulfate, filtered and the solvent removed to yield a tan solid (4.51 g). This solid was recrystalized from a mixture of toluene and hexane to yield a tan solid (3.34 g, 87%); m.p. 102-105° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06117885
Source datasetuspto-grants-2000_09
ORD IDord-8015ee1d2b6b45d7bb71303fdf3647e9
Source noteuspto-grants-2000_09