HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1943088Generated: November 3, 2026
Benzoyl chloride, 3-(sulfinylamino)- → 3-sulfinylamino-N-[2-ethyl-6-methyl-4-(1,2,2,2-tetrafluoro-1-trifluoromethyl-ethyl)-phenyl]-benzamide
https://huagongshe.com/reaction/1943088
Participants
| Role | Name | HCID | Charge |
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| 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 solution of 3-sulfinylamino-benzoyl chloride (0.033 g, 0.165 mmol) (Example 1.1) in dry deuterochloroform (0.5 ml) was added under stirring at 25° C., a solution of 2-ethyl-6-methyl-4-(1,2,2,2-tetrafluoro-1-trifluoromethyl-ethyl)-phenylamine (0.050 g, 0.165 mmol) (prepared according to EP 1,006,102) in deuterochloroform (0.5 ml). After stirring for 60 hours at 25° C., a sample of the reaction mixture was submitted to 1H-NMR spectroscopy. The desired compound was detected in the reaction mixture together with unreacted starting materials. Integration of the signals showed a conversion of 40%. 1H-NMR (CDCl3, 400 MHz): 8.35 (s, 1H), 8.07 (d, 1H), 7.95 (d, 1H) 7.58 (t, 1H), 7.49 (s, 1H), 7.37 (s, 2H), 2.70 (q, 2H), 2.31 (s, 3H), 1.22 (t, 3H) ppm.
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-c0e6970bcda2492e9e93c95d1a8a67cc |
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| Source note | uspto-grants-2013_03 |
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