Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 460650Generated: October 29, 2026

Boron tribromide → HCID 69497972, compound

https://huagongshe.com/reaction/460650

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
ReactantHCID 69497787HCID 69497787—
SolventDichloromethaneHCID 6344—
ProductHCID 69497972HCID 6949797299.9%

Reaction Conditions

Temperature-40 °C

Reaction Steps

3,5-Dihydro-5-(2′-methoxybenzylidene)-2-methyl-3-phenylimidazol-4-one (1.85 g) was dissolved in dichloromethane (30 ml) and boron tribromide (2 ml) was added dropwise while stirring the mixture at −40° C. Thereafter, the mixture was stirred under ice-cooling for 1 hr, poured into ice water and extracted with chloroform. The organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure to give 3,5-dihydro-5-(2′-hydroxybenzylidene)-2-methyl-3-phenylimidazol-4-one (1.76 g) as red crystals. The crystals and (S)-glycidyl nosylate (1.63 g) were dissolved in dimethylformamide (20 ml) and potassium carbonate (1.74 g) was added. The mixture was heated at 50° C. for 2 hr. The reaction mixture was poured into ice water and extracted with ethyl acetate. The organic layer was washed with saturated aqueous ammonium chloride solution, dried over anhydrous sodium sulfate and concentrated under reduced pressure to give an oily product (2.13 g). This oily product and 4-(naphthalen-2-yl)piperidine were dissolved in methanol (20 ml) and refluxed under heating for 2 hr. After cooling, the solvent was evaporated under reduced pressure and the residue was purified by silica gel column chromatography (chloroform/methanol) to give the title compound (0.45 g) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07196199B2
Source datasetuspto-grants-2007_03
ORD IDord-ad3f24c882ee4061818cfc80668b7ef9
Source noteuspto-grants-2007_03