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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49645Generated: October 29, 2026

Thionyl Chloride → 2,4-Dichloro-3-cyano-5-fluorobenzoyl chloride

https://huagongshe.com/reaction/49645

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant2,4-Dichloro-3-cyano-5-fluorobenzoic acidHCID 10900541—
ReactantHydrogen chloride sulphur dioxideHCID 22338718—
SolventPyridineHCID 1049—
Product2,4-Dichloro-3-cyano-5-fluorobenzoyl chlorideHCID 1430013195.7%

Reaction Steps

4100 ml of thionyl chloride and 41 ml of pyridine were introduced into a stirred apparatus fitted with metering device and gas outlet leading to a scrubber via a reflux condenser, and, at 20° C., 2050 g of 3-cyano-2,4-dichloro-5-fluorobenzoic acid (99.5% strength) were introduced at the rate of hydrogen chloride/sulphur dioxide evolution. At the end of the addition, the mixture was heated to reflux until the evolution of gas ceased. The mixture was then distilled. In the boiling range from 142 to 145° C./10 mbar, 2150 g (95.7% of theory) of 3-cyano-2,4-dichloro-5-fluorobenzoyl chloride were obtained (content according to GC: 98.0%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06706918B2
Source datasetuspto-grants-2004_03
ORD IDord-db20833cfd08478986e3edb813feb9a4
Source noteuspto-grants-2004_03