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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 548962Generated: October 28, 2026

Trifluoromethylsulfonamide → HCID 59683172, compound

https://huagongshe.com/reaction/548962

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoromethylsulfonamideHCID 79001—
ReactantHCID 266341HCID 266341—
ReactantMagnesium monoxideHCID 6850729—
ReactantIodo benzene diacetateHCID 12217721—
CatalystDirhodium tetraacetateHCID 152122—
SolventDichloromethaneHCID 6344—
ProductHCID 59683172HCID 5968317291%

Reaction Steps

2.44 g (10.4 mmol) of 2,2,2-trifluoro-N-(4-methylsulphanylphenyl)acetamide and 2.80 g (18.8 mmol) of trifluoromethylsulphonamide are mixed with 145 ml of dichloromethane. 2.09 g (51.9 mmol) of magnesium oxide, 460 mg (1.04 mmol) of rhodium(II) acetate dimer and 6.68 g (20.75 mmol) of iodobenzene diacetate are added to the mixture. The mixture is stirred at room temperature for 1 hour and then filtered, and the filter cake is washed with dichloromethane. On concentration of the filtrate, crystals separate out and are filtered off with suction and washed with a little dichloromethane. Drying results in 3.60 g (9.42 mmol; yield: 91%) of the product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07943629B2
Source datasetuspto-grants-2011_05
ORD IDord-6e0e543e8ee54d28b79424045cda3610
Source noteuspto-grants-2011_05