Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 279087Generated: October 26, 2026

Hydrochloric Acid → 3-(3,5-Bis(trifluoromethyl)phenylamino)-2-(4-chlorophenylsulfonyl)-3-methylsulfanyl-2-propenenitrile

https://huagongshe.com/reaction/279087

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
ReactantSodium BicarbonateHCID 516892—
Reactant2-(4-Chlorobenzenesulfonyl)acetonitrileHCID 735829—
Reactant3,5-Bis(trifluoromethyl)phenyl isothiocyanateHCID 2733395—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
Product3-(3,5-Bis(trifluoromethyl)phenylamino)-2-(4-chlorophenylsulfonyl)-3-methylsulfanyl-2-propenenitrileHCID 8658373193.6%

Reaction Steps

To a solution of 4-chlorophenylsulfonylacetonitrile (1.10 g, 5.10 mmol) in dry acetone (12 ml) first dry potassium carbonate (1.41 g, 10.2 mmol) and then 3,5-bis(trifluoromethyl)phenyl isothiocyanate (1,44 g, 5.31 mmol) were added. The resulting mixture was stirred at room temperature under nitrogen for 1 h, and then filtered. To the filtrate a solution of sodium hydrogencarbonate (0.86 g) in water (15 ml) and methyl iodide (0.945 ml, 15.3 mmol) was added. The mixture was stirred at room temperature for 3.5 h. Then pH was adjusted to ˜4 with 1N HCl. The precipitate was filtered off and washed with water to give 2.39 g (93%) of the title compound. Recrystallisation could be done from ethyl acetate/heptane 1:3. Mp 150.5-152.5° C. 1H NMR (300 MHz, CDCl3): δ=2.25 (s, 3H), 7.57 (d, 2H), 7.79 (s, 2H), 7.83 (s, 1H), 7.88 (d, 2H), 10.0 (br s, 1H); MA calc for C18H11ClF6N2O2S2: C, 43.17%; H, 2.21%; N, 5.59%. Found: C, 43.25%; H, 2.16%; N, 5.59%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06362205B1
Source datasetuspto-grants-2002_03
ORD IDord-fad4d7cfa295418ca915b590471dc9be
Source noteuspto-grants-2002_03