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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1747300Generated: November 1, 2026

1-Chloromethylnaphthalene → HCID 59497422, compound

https://huagongshe.com/reaction/1747300

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-ChloromethylnaphthaleneHCID 6845—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 59497687HCID 59497687—
SolventEthyl AcetateHCID 8857—
SolventDimethylacetamideHCID 31374—
ProductHCID 59497422HCID 5949742213%

Reaction Conditions

Temperature65 °C

Reaction Steps

To a solution of 3-(6-Cyano-2-oxo-2,3-dihydro-benzimidazol-1-yl)-propionic acid ethyl ester (0.1 g, 0.39 mmol) in DMA (3 mL) were added 1-(chloromethyl)naphthalene (0.1 g, 0.58 mmol) and K2CO3 (0.11 g, 0.81 mmol). The reaction mixture was stirred at 65° C. for 16 h. When the reaction was complete, the reaction mixture was diluted with ethyl acetate and washed with water (×4). The organic phase was dried over Na2SO4 and concentrated. The resulting residue was purified by silica gel prep TLC using 98:2 CH2Cl2:MeOH as an eluent to afford 20 mg (13%) of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150556B2
Source datasetuspto-grants-2015_10
ORD IDord-ce743809a1ed48fc87b037e112392ac8
Source noteuspto-grants-2015_10