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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 585429Generated: October 31, 2026

Potassium Carbonate → HCID 12148622, compound

https://huagongshe.com/reaction/585429

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantBromoacetonitrileHCID 11534—
ReactantHCID 12148621HCID 12148621—
SolventDimethylformamideHCID 6228—
ProductHCID 12148622HCID 1214862262.2%

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of (S)-(+)-1-Phenyl-1,2-dihydro[1,4]oxazino[2,3,4-jk]carbazol-7-ol 0.161 g, 0.534 mmol), bromoacetonitrile (0.074 mL, 1.07 mmol), potassium carbonate (0.148 g, 1.07 mmol), and DMF (2 mL) is stirred at 70° C. for 4 h. Additional bromoacetonitrile (0.074 mL) and potassium carbonate (0.074 g) are then added and the mixture is stirred overnight. Bromoacetonitrile and potassium carbonate (0.074 mL and 0.074 g, respectively) are then added and the temperature is increased to 90° C. The mixture is heated at that temperature for 5.5 h and then allowed to cool and stir overnight, after which the mixture is partitioned between ethyl acetate, aq. ammonium chloride, and brine. The organic layers are dried over magnesium sulfate, concentrated, and the residue is chromatographed on silica gel gel (40 mL) using first CH2Cl2/hexane (1:1) to elute unreacted starting material, and then ethyl acetate/CH2Cl2/hexane (5:45:50) to give 0.113 g of (S)-(+)-2-[(1-phenyl-1,2-dihydro[1,4]oxazino[2,3,4-jk]carbazol-7-yl)oxy]acetonitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06932961B1
Source datasetuspto-grants-2005_08
ORD IDord-3cdb9a42a97b4a24ae19c055096472ca
Source noteuspto-grants-2005_08