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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2068466Generated: November 1, 2026

Dimethyl Sulfoxide → HCID 85603868, compound

https://huagongshe.com/reaction/2068466

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantPotassium IodideHCID 4875—
ReactantBenzene, 2-bromo-1,4-dimethyl-HCID 11121—
ReactantPerfluorodecyl iodideHCID 67920—
CatalystCopperHCID 23978—
SolventDichloromethaneHCID 6344—
ProductHCID 85603868HCID 8560386882%

Reaction Steps

A solution of C10F21I (4.2 g, 6.5 mmol) was added dropwise over 10 min to a stirred mixture of 2-bromo-p-xylene (1 g, 5.4 mmol), copper powder (1.9 g, 29.7 mmol), and DMSO (80 mL) at 130° C. The reaction mixture was subsequently stirred for a further 2 d at this temperature. After cooling to room temperature, it was poured into a beaker containing dichloromethane (50 mL) and saturated potassium iodide solution (50 mL). After filtering, the organic layer was separated, washed with water (3×30 mL), and dried over MgSO4. Recrystallization from hexane gave the product 215 as a white solid (2.7 g, 82%): 1H NMR (300 MHz, CDCl3): 7.31 (1H, s), 7.24 (1H, d, J=8.1 Hz)), 7.17 (1H, d, J=8.1 Hz)), 2.46 (3H, t, J=3.0 Hz)), 2.39 (3H, s); 19F NMR (282 MHz, CDCl3): −81.4, −106.7, −121.1, −121.8, −122.0, −122.9, −126.3; HR-MS (EI) calcd. for C18H9F21 (M+): 624.0363, found: 624.0353.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08298830B2
Source datasetuspto-grants-2012_10
ORD IDord-96d8c2b55d7f42a69625c6500b106964
Source noteuspto-grants-2012_10