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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1859790Generated: November 1, 2026

Dichloromethane → HCID 178479625, compound

https://huagongshe.com/reaction/1859790

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantPotassium CarbonateHCID 11430—
Reactant6-Hydroxy-3,4-dihydro-1(2H)-naphthalenoneHCID 4679494—
ReactantHCID 178419249HCID 178419249—
SolventDimethylformamideHCID 6228—
Solvent2-OxopropiononitrileHCID 69430—
ProductHCID 178479625HCID 17847962533%

Reaction Steps

6-Hydroxytetralone (1.46 g, 9.01 mmol) was dissolved in a mixture of 15 mL AcCN and 8 mL DMF, and solid potassium carbonate (4.98 g, 36 mmol) was added followed by a solution of 4-(2-bromoethyl)-1H-imidazole hydrobromide (2.05 g, 8.01 mmol) in a mixture of 15 mL AcCN and 3 mL DMF. After stirring for 24 hours at room temperature, the reaction was concentrated in vacuo to remove the solvents, and the resulting residue was diluted with water and extracted into EtOAc. The pooled organics were washed sequentially with a saturated solution of NaHCO3, water, and brine and concentrated in vacuo to afford 1.57 g of crude product. Purification by flash chromatography (silica gel, 235 g, 5% MeOH in DCM) gave a yellow oil. The oil was taken up in 7 mL DCM, and the product was precipitated as a salt by the addition of 1.5 mL of 8N HCl in iPrOH. The solid was collected, washed with iPrOH, triterated with Et2O, and dried in vacuo to afford 0.826 g (33%) of the title compound;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06528535B2
Source datasetuspto-grants-2003_03
ORD IDord-4c26f8ebd27b4396ace80cf4f975e216
Source noteuspto-grants-2003_03