Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1171706Generated: November 1, 2026

Dichloromethane → HCID 23138491, compound

https://huagongshe.com/reaction/1171706

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 23139177HCID 23139177—
SolventEthanolHCID 702—
ProductHCID 23138491HCID 2313849137.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

Sodium borohydride (0.06 g) was added to a solution of (E)-3-{[1-(ethoxycarbonylmethyl)-1H-imidazol-5-yl]methylidene}-1-(triphenylmethyl)piperidin-4-one (1.5 g) in a mixed solvent of dichloromethane (10 ml) and ethanol (10 ml) at 0° C. After the mixture was stirred at 0° C. for 0.5 hour and then at room temperature for 1.5 hour, it was partitioned between water and ethyl acetate. The organic layer was separated, washed with a saturated aqueous sodium chloride solution and dried over anhydrous magnesium sulfate. Removal of the solvent under reduced pressure followed by purification of the residue by silica gel chromatography using dichloromethane and methanol (19:1) as an eluent to give the title compound (560 mg, yield: 37%) as a yellow amorphous solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07829580B2
Source datasetuspto-grants-2010_11
ORD IDord-0b5cedfe96d54ee7a9eea08de63a17da
Source noteuspto-grants-2010_11