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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

Reaction equation

Participants

RoleNameHCIDCharge
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 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08389767B2
Source datasetuspto-grants-2013_03
ORD IDord-c0e6970bcda2492e9e93c95d1a8a67cc
Source noteuspto-grants-2013_03