Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1173481Generated: November 2, 2026

Benzoyl chloride → HCID 11582406, compound

https://huagongshe.com/reaction/1173481

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantHCID 86623740HCID 86623740—
SolventDichloromethaneHCID 6344—
ProductHCID 11582406HCID 1158240666.4%

Reaction Steps

A solution of crude 4-[(2-aminoethyl)(2,2,2-trifluoroethyl)amino]-2-(trifluoromethyl)benzonitrile (0.018 mg, 0.058 mmol) in CH2Cl2 (3 mL) was treated with TEA (0.0064 g, 0.063 mmol) and benzoyl chloride (0.0089 mg, 0.063 mmol) and stirred at rt for 1 h. The mixture was partitioned between EtOAc and 0.1N HCl. The organic phase was washed with 0.1N HCl and brine, dried (Na2SO4) and concentrated in vacuo. The residue was purified by silica gel chromatography (5-70% EtOAc/hexanes gradient) and the product crystallized from CH2Cl2/hexanes to give the title compound as a white solid (0.016 g, 66% yield): MS (ES) mlz 416 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07834063B2
Source datasetuspto-grants-2010_11
ORD IDord-af594ab29c254051af25ec027acc7572
Source noteuspto-grants-2010_11