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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1168671Generated: November 1, 2026

2,5-Difluorobenzoyl chloride → HCID 69314684, compound

https://huagongshe.com/reaction/1168671

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,5-Difluorobenzoyl chlorideHCID 588082—
ReactantHCID 22270286HCID 22270286—
SolventDichloromethaneHCID 6344—
ProductHCID 69314684HCID 6931468474%

Reaction Steps

2,5-difluorobenzoylchloride 1.5 eq is treated with 1.0 eq 1.25 g (3.3 mmole) of propyl({1-propyl-5-[(1,1,2,2-tetramethyl-1-silapropoxy)methyl]benzimidazol-2-yl}methyl) amine in dichloromethane at room temperature for 1 hr. The reaction is quenched with 1 N NaOH and partitioned between dichloromethane and water. The organic layer is dried over anhydrous Na2SO4 and the solvent removed in vacuo. The residue is chromatographed (SiO2) with ethyl acetate to afford 74% of (2,5-difluorophenyl)-N-propyl-N-({1-propyl-5-[(1,1,2,2-tetramethyl-1-silapropoxy)methyl]benzimidazol-2-yl}methyl)carboxamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06627624B1
Source datasetuspto-grants-2003_09
ORD IDord-c920ac9e5b044096be150078f0afd166
Source noteuspto-grants-2003_09