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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Benzoyl chloride, 3-(sulfinylamino)- | HCID 12238911 | — |
| Reactant | 2-Methyl-6-ethyl-4-(heptafluoro-prop-2-yl)-aniline | HCID 22734610 | — |
| Solvent | Chloroform-D | HCID 71583 | — |
| Product | 3-sulfinylamino-N-[2-ethyl-6-methyl-4-(1,2,2,2-tetrafluoro-1-trifluoromethyl-ethyl)-phenyl]-benzamide | HCID 44475037 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08389767B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-d2b661495f5e4808a418543006c51a52 |
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| Source note | uspto-grants-2013_03 |
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