Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 277689Generated: October 25, 2026

Tert-Butylbenzene → HCID 22625489, compound

https://huagongshe.com/reaction/277689

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-ButylbenzeneHCID 7366—
ReactantIodosylbenzeneHCID 92125—
Reactant1-Propanesulfonic acid, 1,1,2,3,3,3-hexafluoro-HCID 9794628—
SolventDichloromethaneHCID 6344—
ProductHCID 22625489HCID 22625489—

Reaction Conditions

Temperature0 °C

Reaction Steps

4.4 g (20 mmol) of iodosylbenzene was suspended in 100 ml of dry dichloromethane. The suspension was cooled to 0° C. with stirring. 4.65 g (20 mmol) of 3,3,3,2,1,1-hexafluoropropane sulfonic acid (optionally distilled) was added at the same temperature thereto under exclusion of moisture. The mixture was stirred at room temperature for 3 hours. The temperature of the mixture was returned to 0° C., and 2.68 g (20 mmol) of 4-t-butylbenzene was added thereto at that temperature. The temperature of the mixture was returned to room temperature, followed by stirring for 6 hours. Thereafter, the insolubles were removed by filtration. The solvent was removed from the filtrate. The oily residue was purified by recrystallization (twice) from diethyl ether. The structure was confirmed by 1H-NMR (CDCl3): δ=0.81 (s, 9H), 4.98-5.22 (m[d], 1H), 7.18-7.23 (d, 2H), 7.58-7.65 ppm (m, 7H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06358665B1
Source datasetuspto-grants-2002_03
ORD IDord-10b1fad91dc64ce68db68fd3e18524a1
Source noteuspto-grants-2002_03