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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49955Generated: October 26, 2026

2-Fluoro-5-(trifluoromethyl)aniline → 3-Ethoxythiocarbonylthio-4-fluorobenzotrifluoride

https://huagongshe.com/reaction/49955

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Fluoro-5-(trifluoromethyl)anilineHCID 136349—
ReactantPotassium ethylxanthateHCID 2735045—
ReactantSodium NitriteHCID 23668193—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
Product3-Ethoxythiocarbonylthio-4-fluorobenzotrifluorideHCID 1209735399%

Reaction Conditions

Temperature-59 °C

Reaction Steps

2-Fluoro-5-trifluoromethylaniline (14 g) was suspended in 30 ml of water and 10 ml of concentrated hydrochloric acid. The suspension was cooled to −5° C. while a solution of 5.93 g of sodium nitrite in 30 ml of water was added dropwise, followed by stirring at −59° C. for 2 hours. Then the solution was added to a solution of 16 g of potassium O-ethyl dithiocarbonate in 20 ml of water (40 to 50° C.), followed by stirring for 1 hour. The reaction mixture was extracted with an aqueous solution of ethyl acetate, dried and concentrated, giving 22 g of 3-ethoxythiocarbonylthio-4-fluorobenzotrifluoride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06710062B1
Source datasetuspto-grants-2004_03
ORD IDord-0f9fecd1643e4add9ad5763b945bc4a1
Source noteuspto-grants-2004_03