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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1749128Generated: November 1, 2026

Benzenamine, 3,5-bis(trifluoromethyl)- → HCID 75202965, compound

https://huagongshe.com/reaction/1749128

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenamine, 3,5-bis(trifluoromethyl)-HCID 9480—
Reactant4-tert-butyl-2,6-dimethylbenzenesulfonyl chlorideHCID 3868506—
SolventPyridineHCID 1049—
ProductHCID 75202965HCID 7520296523%

Reaction Steps

4-Tert-butyl-2,6-dimethyl-benzenesulfonyl chloride (0.100 g, 0.383 mmol) was added to a solution of 3,5-bis(trifluoromethyl)aniline (0.089 g, 0.387 mmol) in dry pyridine (1 mL). The reaction was capped and stirred at room temperature for 1 day then stirred at 30° C. for 1 day. The reaction was then concentrated under vacuum. To this was added diethyl ether (60 mL) and the mixture was washed with 0.1 N HCl (3×20 mL) followed by 0.1 N NaOH (2×20 mL) then saturated NaCl (2×20 mL). After drying the organic layer over MgSO4, the solution was filtered and concentrated under vacuum. The crude compound was triturated with hexanes (2×10 mL) to afford the title compound (0.040 g, 23% yield). LCMS (M+Na) 476.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156781B2
Source datasetuspto-grants-2015_10
ORD IDord-5d1214be971c41559278d12286f84a74
Source noteuspto-grants-2015_10