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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 843663Generated: October 30, 2026

2,5-Difluorobenzoyl chloride → HCID 69314684, compound

https://huagongshe.com/reaction/843663

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 numberUS06380210B1
Source datasetuspto-grants-2002_04
ORD IDord-170390ebc67643a3a5b5dbcb42d80188
Source noteuspto-grants-2002_04