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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1057647Generated: November 4, 2026

Potassium Carbonate → HCID 18671666, compound

https://huagongshe.com/reaction/1057647

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantBromoacetonitrileHCID 11534—
ReactantHCID 18671656HCID 18671656—
SolventDimethylformamideHCID 6228—
ProductHCID 18671666HCID 18671666113.9%

Reaction Conditions

Temperature85 °C

Reaction Steps

A mixture of 9-benzyl-3-chloro-9H-carbazol-4-ol (0.227 g, 0.739 mmol), bromoacetonitrile (0.177 g, 1.48 mmol), potassium carbonate (0.204 g, 1.48 mmol), and DMF (2 mL) is heated at 85° C. for 4 h, then allowed to cool and stir at room temperature for 12 h. Additional bromoacetonitrile (0.177 g) and potassium carbonate (0.204 g) are added and the mixture is heated again at 85° C. for 2 h. After cooling, the mixture is combined with that from another experiment run in the same manner (starting with 0.15 g of 9-benzyl-3-chloro-9H-carbazol-4-ol) and the combined mixtures are partitioned between ethyl acetate-aq. ammonium chloride/brine and brine. The organic layer is dried over magnesium sulfate and concentrated to dryness. Chromatography on silica gel (55 mL) using ethyl acetate-hexane (10/90) gave 0.292 g of [(9-benzyl-3-chloro-9H-carbazol-4-yl)oxy]acetonitrile as a clear liquid. 1H NMR (CDCl3) δ5.07, 5.50, 7.11, 7.15, 7.25-7.47, 7.50, 8.34.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06514968B1
Source datasetuspto-grants-2003_02
ORD IDord-c00082179b724079ac1d7b9d9eb67a87
Source noteuspto-grants-2003_02