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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1264335Generated: November 1, 2026

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

https://huagongshe.com/reaction/1264335

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 numberUS06541675B2
Source datasetuspto-grants-2003_04
ORD IDord-03199c8032fe4d1caa078896646bb181
Source noteuspto-grants-2003_04