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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 554086Generated: October 25, 2026

Ammonia → 2-Chloro-3,4-difluorobenzamide

https://huagongshe.com/reaction/554086

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantThionyl ChlorideHCID 24386—
Reactant2-Chloro-3,4-difluorobenzoic acidHCID 10012817—
Solvent1,4-DioxaneHCID 31275—
Product2-Chloro-3,4-difluorobenzamideHCID 59370545—

Reaction Conditions

Temperature80 °C

Reaction Steps

2-Chloro-3,4-difluorobenzoic acid (2 g, 10.4 mmol) was treated with thionyl chloride (3.04 ml) and the mixture was heated to 80° C. for 90 minutes. The mixture was then cooled and reduced in vacuo. The residue was dissolved in anhydrous 1,4-dioxane (10 ml) and the mixture was then cooled in an ice-water bath. 0.88 Ammonia (aqueous, 25 ml) was added dropwise to the mixture which was subsequently allowed to warm to 22° C. over a period of 2 hrs. This process was repeated using 10.8 g of 2-chloro-3,4-difluorobenzoic acid, 8.2 ml of thionyl chloride, and 45 ml of 0.88 ammonia and then both mixtures were combined and partitioned between ethyl acetate (150 ml) and water (100 ml). The aqueous layer was separated and extracted with 2×150 ml aliquots of ethyl acetate. The combined organic extracts were then washed with saturated aqueous sodium hydrogen carbonate (100 ml), dried using a hydrophobic frit, and reduced in vacuo to give 2-chloro-3,4-difluorobenzamide (11.86 g) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08048907B2
Source datasetuspto-grants-2011_11
ORD IDord-c9760b5808534ad7858b7156d03c157e
Source noteuspto-grants-2011_11