Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 644549Generated: October 29, 2026

Formate → N,N-Diethyl-3-(3-Phenyl-6-trifluoromethyl-3H-benzimidazol-4-yl)propionamide

https://huagongshe.com/reaction/644549

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormateHCID 283—
ReactantHCID 68679532HCID 68679532—
CatalystChlorotris(triphenylphosphine)rhodium(I)HCID 84599—
SolventDimethyl SulfoxideHCID 679—
ProductN,N-Diethyl-3-(3-Phenyl-6-trifluoromethyl-3H-benzimidazol-4-yl)propionamideHCID 68679691—

Reaction Steps

Alumina supported formate was prepared according to the procedure of Danks and Desai (T. N. Danks and B. Desai, Green Chemistry, 2002, 4, 179-180). A Smith Process Vial™ was loaded with alumina supported formate (0.5 g), Wilkinson's catalyst (0.5 mg), N,N-diethyl-3-(3-phenyl-6-trifluoromethyl-3H-benzimidazol-4-yl)acrylamide (0.064 mmol, 25 mg) and dimethylsulphoxide (0.5 ml) and was irradiated for 600 s at 180° C. using a Personal Chemistry Smith Creator™ microwave. The mixture was filtered to remove the solid support and the filtrate was purified by LCMS to give, after evaporation, the title compound as a solid (7.8 mg, 31%), m/z 390.0 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07700638B2
Source datasetuspto-grants-2010_04
ORD IDord-f2302d38c54e4a279d503166b3412e9e
Source noteuspto-grants-2010_04