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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 488407Generated: October 28, 2026

Thionyl Chloride → HCID 11316097, compound

https://huagongshe.com/reaction/488407

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 131723205HCID 131723205—
ProductHCID 11316097HCID 1131609793%

Reaction Steps

(2,5-difluorophenyl)-N-{[5-(hydroxymethyl)-1-propylbenzimidazol-2-yl]methyl}-N-propylcarboxamide 0.96 g (2.3 mmole) is treated with 30 mL of thionyl chloride for 15 min a room temperature. The resulting mixture is concentrated in vacuo and partitioned between 100 mL sat NaHCO3 and 100 mL of ethyl acetate. The ethyl acetate layer is dried over anhydrous Na2SO4 and concentrated in vacuo. The resulting oil is chroamtoagraphed 50% ethyl acetate/hexanes to afford 0.9 g (93%) of (2,5-difluorophenyl)-N-{[5-(chloromethyl)-1-propylbenzimidazol-2-yl]methyl}-N-propylcarboxamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06972293B2
Source datasetuspto-grants-2005_12
ORD IDord-21525dedce8d4a3280e4e344cbd35909
Source noteuspto-grants-2005_12