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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2080506Generated: November 2, 2026

Water → HCID 58734278, compound

https://huagongshe.com/reaction/2080506

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium ethylxanthateHCID 2735045—
Reactant5-Amino-2-(trifluoromethyl)pyridineHCID 2737744—
ReactantSodium NitriteHCID 23668193—
SolventHydrochloric AcidHCID 313—
SolventMethanolHCID 887—
SolventHexaneHCID 8058—
ProductHCID 58734278HCID 5873427856%

Reaction Conditions

Temperature65 °C

Reaction Steps

After 6-trifluoromethylpyridin-3-ylamine (1.00 g, 6.02 mmol) was dissolved in 1N hydrochloric acid (15 ml) and methanol (3 ml), a water (3 ml) solution of sodium nitrite (506 mg, 7.22 mmol) was added dropwise to the resulting solution at −10° C. The reaction mixture was added dropwise to a water (15 ml) solution of potassium o-ethyl dithiocarbonate (1.93 g, 12.0 mmol) heated to 65° C. At the same temperature, the reaction mixture was stirred for 30 minutes. After the reaction mixture was cooled to room temperature, the product thus obtained was extracted with ethyl acetate. The extract was washed with brine. The organic layer was dried over anhydrous sodium sulfate, and filtered. The filtrate was concentrated under reduced pressure. The residue thus obtained was subjected to flash silica gel column chromatography. The fraction obtained from the hexane:ethyl acetate=100:1 eluate was concentrated under reduced pressure to give the title compound (895 mg, 3.35 mmol, 56%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07932271B2
Source datasetuspto-grants-2011_04
ORD IDord-a5f89d74079743c5a83e6ac2fbe5539c
Source noteuspto-grants-2011_04