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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1943090Generated: October 27, 2026

Potassium Carbonate → 3-sulfinylamino-N-[2-ethyl-6-methyl-4-(1,2,2,2-tetrafluoro-1-trifluoromethyl-ethyl)-phenyl]-benzamide

https://huagongshe.com/reaction/1943090

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantBenzoyl chloride, 3-(sulfinylamino)-HCID 12238911—
Reactant2-Methyl-6-ethyl-4-(heptafluoro-prop-2-yl)-anilineHCID 22734610—
SolventChloroform-DHCID 71583—
Product3-sulfinylamino-N-[2-ethyl-6-methyl-4-(1,2,2,2-tetrafluoro-1-trifluoromethyl-ethyl)-phenyl]-benzamideHCID 44475037—

Reaction Conditions

Temperature25 °C

Reaction Steps

To a suspension of 2-ethyl-6-methyl-4-(1,2,2,2-tetrafluoro-1-trifluoromethyl-ethyl)-phenylamine (0.082 g, 0.27 mmol) (prepared according to EP 1,006,102) and finely ground potassium carbonate (0.112 g, 0.81 mmol) in deuterochloroform (1.0 ml) under stirring at 25° C., was added 3-sulfinylamino-benzoyl chloride (0.055 g, 0.27 mmol) (Example 1.1) dissolved in dry deuterochloroform (1.0 ml). The reaction mixture was stirred at 40° C. for 16 hours. A sample of the supernatant was submitted to 1H-NMR spectroscopy. The desired compound was detected in the reaction mixture, based on its characteristic signals (see 1H-NMR spectral data as described in Example 2.2), together with unreacted starting materials. An aliquot of the reaction mixture was diluted in dry acetonitrile and was submitted to mass spectrometry via direct injection (same conditions as described in Example 2.1). Calculated exact mass: 468; [M-H]− observed: 467.00.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08389767B2
Source datasetuspto-grants-2013_03
ORD IDord-d2b661495f5e4808a418543006c51a52
Source noteuspto-grants-2013_03