Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1817214Generated: October 30, 2026

Potassium Carbonate → HCID 11716432, compound

https://huagongshe.com/reaction/1817214

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantTrimethylsilyl cyanideHCID 82115—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant1-Azabicyclo[2.2.2]oct-4-yl(diphenyl)methanolHCID 23992385—
Solvent1,2-DichloroethaneHCID 11—
SolventEthyl AcetateHCID 8857—
ProductHCID 11716432HCID 1171643259.7%

Reaction Conditions

Temperature85 °C

Reaction Steps

To a suspension of 1-azabicyclo[2.2.2]oct-4-yl(diphenyl)methanol (0.3055 g, 1.04 mmol) in 1,2-dichloroethane (17 mL) was added AlCl3 (0.6675 g, 5.04 mmol). The reaction was allowed to stir for 10 min and then TMSCN (0.68 mL, 5.10 mmol) was added. The reaction was sealed and heated to 85° C. for overnight. The reaction mixture was poured into a separatory funnel containing K2CO3 (aq. sat.) (100 mL) and EtOAc (100 mL). The aqueous phase was separated and further extracted with EtOAc (3×100 mL) was performed. The combined organics were dried over MgSO4, filtered and concentrated under vacuum. The residue was dissolved in DMSO and purified by Gilson preparatory HPLC (w/0.1% TFA). The combined fractions were concentrated down under vacuum to remove CH3CN. The resulting water layer was basified to pH=12 with 6N NaOH, and then extracted with EtOAc. The combined organic fractions were dried over MgSO4, filtered, and concentrated under vacuum to give the title compound (0.185 g, 59.7%). EI-MS ml/z 303 (M+H+) Rt (1.76 min).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07598267B2
Source datasetuspto-grants-2009_10
ORD IDord-826fdc2d67a24f6095e9654074e137d1
Source noteuspto-grants-2009_10