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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2098997Generated: October 31, 2026

Sulfuric Acid → 3-Chloro-2-fluorophenol

https://huagongshe.com/reaction/2098997

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
Reactant3-Chloro-2-fluoroanilineHCID 75014—
ReactantSodium NitriteHCID 23668193—
CatalystCopper SulfateHCID 24462—
SolventTolueneHCID 1140—
Product3-Chloro-2-fluorophenolHCID 277371240.9%

Reaction Conditions

Temperature80 °C

Reaction Steps

728 g of 3-chloro-2-fluoroaniline was added to a reactor having 6,860 g of 30.6% sulfuric acid placed therein, followed by stirring for 30 minutes at 80° C. Thereafter, the mixture was cooled to −10° C., and 952 g of a 37.0% sodium nitrite aqueous solution was added dropwise thereto over 90 minutes in a temperature range of −10 to −5° C., followed by stirring for 30 minutes in that temperature range. The resulting reaction mixture was added to another reactor having 4,100 g of 51.2% sulfuric acid, 1,500 g of copper sulfate and 3,000 mL of toluene placed therein over 6 hours in a temperature range of 80 to 85° C., followed by stirring for 30 minutes in that temperature range. The resulting reaction mixture was cooled to a temperature range of 70 to 75° C. and left at rest to separate into two layers, i.e., an organic layer and an aqueous layer, and the organic layer was collected. The aqueous layer was cooled to 20° C., and copper sulfate was filtered off, followed by extracting with 1,200 mL toluene twice. The organic layer obtained by extraction was washed with 700 mL of water and subjected to fractional distillation to obtain 300 g of 3-chloro-2-fluorophenol (b5). The compound had a boiling point of 60 to 62° C./1 mmHg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07569258B2
Source datasetuspto-grants-2009_08
ORD IDord-a1142ac226b344778c8ebfaa2fdbfbc3
Source noteuspto-grants-2009_08