Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1471010Generated: October 30, 2026

4-Aminophenyl trifluoromethyl sulphone → HCID 67236489, compound

https://huagongshe.com/reaction/1471010

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Aminophenyl trifluoromethyl sulphoneHCID 136315—
Reactant1,4-Bis(4-bromophenyl)-1,4-butanedioneHCID 219217—
CatalystTitanium TetrachlorideHCID 24193—
SolventTolueneHCID 1140—
ProductHCID 67236489HCID 6723648968%

Reaction Steps

To a slurry of the product from Example 26E (0.60 g, 1.52 mmol) and 4-(trifluoromethylsulfonyl)aniline (0.51 g, 2.27 mmol) in toluene (12 mL) was added a 1N solution of titanium(IV) chloride (1.6 mL, 1.6 mmol) in toluene. The mixture was stirred overnight at room temperature and then heated to reflux for 3 hours. The cooled mixture was filtered and the solid residue was suspended in a mixture of water and diethyl ether. The solid was diluted with water and ether and stirred vigorously for 15 minutes. The mixture was filtered and then washed thoroughly with diethyl ether to give the title compound as a crude mixture that was used in subsequent reactions without further purification (0.60 g, 68% yield crude).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09006387B2
Source datasetuspto-grants-2015_04
ORD IDord-53cc263a7f814180ba238897694a0412
Source noteuspto-grants-2015_04